BSE Feed Ban Enhancement: Implementation Questions and Answers Updated March 10, 2009

Feed Ban Enhancement: Implementation Questions and Answers Updated March 10, 2009

Feed Ban Enhancement: Implementation Questions and Answers Updated March 10, 2009

The 2008 Regulation

1. Q: What changes were made to FDA’s animal feed regulations?

A: The changes to the regulations provide additional protections against bovine spongiform encephalopathy (BSE, “mad cow disease”). FDA added a new section 589.2001 to the regulations which prohibits the use of high-risk cattle material in feed for all animal species. This section builds on the 1997 BSE feed regulation at 589.2000, which remains in effect but which applies only to feed for cattle and other ruminants. Specifically, the new section 589.2001 defines the following as cattle material prohibited in animal feed (CMPAF):

the entire carcass of BSE-positive cattle

the brains and spinal cords from cattle 30 months of age and older

the entire carcass of cattle not inspected and passed for human consumption, unless the cattle are less than 30 months of age or the brains and spinal cords have been effectively removed

tallow derived from BSE-positive cattle

tallow derived from CMPAF that contains more than 0.15% insoluble impurities

mechanically separated beef derived from CMPAF

2. Q: Were any changes made to section 589.2000?

A: Yes. The definition of protein derived from mammalian tissue was changed to exclude tallow containing no more than 0.15% insoluble impurities. This means that tallow containing more than 0.15% insoluble impurities may no longer be fed to cattle and other ruminants. [See Comment 33 and 589.2000(a)(1) page 22756]

3. Q: What is the impact of the new regulation on feed manufacturers?

A: The primary impact of the 2008 rule will be on the rendering industry due to a number of specific requirements for renderers. However, feed manufacturers may be impacted by the requirement in the new rule that animal feed and feed ingredients shall not be manufactured from, processed with, or otherwise contain CMPAF. In addition, the change to section 589.2000 means that feed manufacturers will need to make sure that tallow used in ruminant feed contains not more than 0.15% insoluble impurities.

4. Q: Will the FDA provide a period of time after the effective date (like that given for the 1997 rule) to educate renderers about new requirements under the 2008 rule?

A: No. The 12-month implementation period is intended to provide sufficient time for the industry to become familiar with the requirements of the rule.

5. Q: Does the definition of CMPAF apply to material derived from livestock other than cattle?

A: The new rule applies only to cattle (bos taurus, bos indicus) and buffalo (bison bison) and not to other livestock species such as sheep, swine, or horses. The rule may have an indirect impact on how renderers handle other species, depending on how individual rendering companies respond to the rule.

Exclusions

6. Q: Will FDA list specific exclusions from the rule such as poultry fat, pork fat, recycled restaurant grease (from food offered for human consumption), and blood products to help prevent market disruptions?

A: No. This rule is clear in defining CMPAF and does not restrict the use of any other products in animal feed.

Implementation

7. Q: When does the new regulation go into effect?

A: The regulation becomes effective on April 27, 2009, one year after publication in the Federal Register. The 12-month implementation period allows time for the livestock, meat, rendering, and animal feed industries to adapt their practices to comply with the new regulation.

8. Q: What about feed manufactured before April 27, 2009 that contains CMPAF?

A: After April 27, 2009 it will not be legal to introduce into interstate commerce feed or feed ingredients containing CMPAF. Because the rule does not provide a grace period for using up feed made with CMPAF, it is expected that renderers and feed manufacturers will discontinue use of materials containing CMPAF in time to ensure that feed in distribution after the deadline is free of CMPAF.

9. Q: When will more detailed guidance be available for renderers, feed manufacturers and livestock producers?

A: Additional guidance can be found in Draft Guidance for Industry #195, which can be found on the CVM website at http://www.fda.gov/cvm/bsetoc.html .

Disposal of CMPAF

10. Q: Can older dead stock cattle and byproducts from meat packing plants that slaughter older cattle still be used in animal feed for non-ruminants?

A: Yes, as long as the material is free of CMPAF.

11. Q: What is going to happen to the CMPAF that can no longer be used in animal feed?

A: A number of methods are currently available for disposing of CMPAF, including landfill, incineration, composting, alkaline hydrolysis, and burial. Another disposal option is to first render CMPAF to stabilize the material and reduce the volume, and then dispose of the rendered material by means other than use in animal feed. Whatever methods are used to dispose of CMPAF, they must comply with state and local requirements.

12. Q: Can ash from the incineration of CMPAF be used in feed?

A: No. The rule prohibits the use of CMPAF in animal feed and does not contain any provisions allowing for inactivation of BSE infectivity.

13. Q: Can CMPAF be rendered for use as fertilizer?

A: This rule does not place any restrictions on the use of CMPAF as fertilizer.

By-products from slaughter establishments

14. Q: How will renderers be assured that cattle offal received from slaughter facilities does not contain CMPAF?

A: Renderers must have records that demonstrate that establishments supplying cattle material to the renderer have adequate procedures in place to exclude CMPAF. These records will be considered sufficient if they include certification or other documentation from the supplier that material supplied to the renderer does not contain CMPAF, or documentation of another method acceptable to FDA, such as third-party certification. [See Section C page 22735]

15. Q: What does an acceptable certification consist of?

A: Certification is acceptable, provided it includes a description of the supplier’s segregation procedures, documentation that the supplier confirms that its segregation procedures were in place prior to supplying any cattle material to the renderer, and records of the renderer’s periodic review of the suppliers’ certification or documentation of another method acceptable to FDA, such as a third party certification, for verifying that suppliers have effectively excluded CMPAF. [Section C page 22735]

16. Q: The rule requires periodic review of the suppliers’ certification. How often is periodic?

A: The rule does not specify a frequency.

17. Q: A firm’s written procedures are typically proprietary, so how extensive does the description of procedures need to be?

A: The rule does not specify how detailed the description must be. However, with respect to cattle materials obtained from establishments which have segregated CMPAF, such records must demonstrate that those establishments supplying cattle materials to the renderer have adequate procedures in place to effectively exclude CMPAF.

18. Q: How does FDA expect renderers to review the suppliers’ certification or other documentation? Will certification renewal be adequate? Does FDA expect renderers to audit supplier documents and procedures – such access will most likely be denied and FDA has limited authority over such suppliers?

A: The rule does not specify the requirements of a review.

19. Q: Who is responsible if it is determined that CMPAF was not excluded from slaughter offal used to produce MBM for animal feed use?

A: Although all parties are expected to exercise due diligence in excluding CMPAF, the rule places the responsibility on the renderer.

20. Q: Will a renderer be responsible for a recall if a supplier of raw material did not remove CMPAF?

A: If it is determined that material rendered for animal feed use contains CMPAF and a recall is necessary, the renderer would be responsible for conducting the recall. However, establishing liability for the cost of the recall should not be different than for other customer/supplier business relationships.

21. Q: How will the new rule be enforced at small slaughtering facilities?

A: Inspections will not be conducted at any slaughter establishments, regardless of size. Inspections will be conducted at rendering facilities to verify that the renderer has determined that CMPAF is being excluded from inedible raw materials supplied by slaughter establishments.

22. Q: Are all specified risk materials (SRMs) required to be separated, or just the brains and spinal cords from cattle over 30 months?

A: The rule requires separation of those materials defined by the rule as CMPAF. In a slaughter facility, this means the brain and spinal cord from any animal over 30 months of age. As explained in the preamble to the 2008 rule, FDA does not believe it is necessary to prohibit from use in feed for non-ruminants any other tissues defined elsewhere (e.g. by OIE or USDA) as SRMs.

23. Q: Does the rule require suppliers of raw material to renderers to be trained and certified on handling their CMPAF?

A: No. FDA intends to provide outreach explaining the requirements of the rule, but does not intend to provide training to the private sector.

24. Q: What items specifically will not be accepted by renderers as a result of this new rule?

A: The rule does not prohibit a renderer from accepting any of the items they may currently be accepting; the rule prohibits the rendering of CMPAF for use in animal feed. Individual rendering establishments will determine what they choose to accept for further processing. A renderer may choose to collect CMPAF for disposal, as a service to slaughter establishments.

25. Q: Will the FDA develop a standard report to be used in recording CMPAF and/or non-CMPAF material from various sources? It would be helpful if all suppliers and all renderers use the same form for supplier certification.

A: No. FDA will not be developing a standard form, but the rule does not prevent a standard form from being used if industry chooses to develop one.

State-Inspected and Custom Slaughter Facilities

26. Q: Are cattle that are slaughtered in state-inspected facilities eligible for rendering for feed use?

A: Yes. 21 FR 589.2001(b)(2) defines “cattle not inspected and passed for human consumption” as cattle that did not pass antemortem inspection by the appropriate regulatory authority. In a state-inspected slaughter facility the state is the appropriate regulatory authority and animals that pass antemortem inspection may be rendered for use in animal feed provided that other requirements of the rule, such as removal of brain and spinal cord from animals over 30 months of age, are met.

27. Q: Can cattle offal from uninspected (custom) slaughter be rendered for feed use?

A: Yes. Cattle slaughtered under custom slaughter meet the definition of “cattle not inspected and passed for human consumption”. Therefore, offal from custom slaughter operations may be rendered for feed use if the brain and spinal cord from cattle older than 30 months are excluded from the offal. Just as they would for an inspected slaughter establishment, renderers receiving material from a custom slaughter operation would need records that demonstrate that the establishment has adequate procedures in place to exclude CMPAF. [See comments 38 and 57]

Determining Age of Cattle

28. Q: How will renderers determine and document the age of cattle not inspected and passed for human consumption (e.g., dead stock cattle) that are collected to be rendered for feed use?

A: Renderers are required to maintain written procedures for specifying how they either remove brain and spinal cord from cattle not inspected and passed for human consumption, or how they separate such animals based on whether they are 30 months of age or older. Written procedures must be made available for FDA inspection. [See 589.2001(c)(2)(ii) and comments 30 and 40]. Additional information is available in Draft Guidance for Industry #195.

29. Q: What are acceptable procedures for determining the age of cattle?

A: As discussed in the preamble to this rule, FDA received a number of suggestions for ways to determine the age of cattle, including animal identification systems, dairy herd records, dentition, body weight, or feedlot origin. The rule requires only that renderers have written procedures explaining how they determine the age of cattle they process as well as records documenting their compliance with the requirement. It does not mandate the use of a specific method of determining the age of the cattle. [See 589.2001(c)(2)(ii) and comments 30 and 40]. Additional information is available in Draft Guidance for Industry #195.

30. Q: Can renderers accept farmer statements based on production records?

A: Yes, as long as the records meet the requirements in 589.2001(c)(3)(i) (A) or (B).

31. Q: What kinds of written documentation for age verification will be acceptable? Will a handwritten note, signed and dated by the owner, suffice?

A: Nothing in the rule prevents this form of documentation if it meets the requirements in 589.2001(c)(3)(i) (A) or (B).

32. Q: Will renderers be held liable for mistakes in statements of age?

A: Although all parties are expected to exercise due diligence in complying with the rule, the rule places the responsibility on the renderer. The renderer is expected to have procedures in place that will minimize the potential for mistakes. For example, a renderer may wish to use dentition to confirm that the producer’s statement is correct. [See comment 28, comment 40; also 589.2001(c)(2)(ii) and 589.2001(c)(3)(i)]

33. Q: Will dentition be accepted as a determinant of age of cattle?

A: Nothing in the rule prevents the use of dentition as a method for determining the age of cattle. We are aware that under USDA procedures for using dentition, cattle are considered to be 30 months of age or older if at least one of the second set of permanent incisors has erupted through the gum line. [See Comment 40]

34. Q: Will renderers be required to provide training on using dentition to determine the age of cattle?

A: No.

35. Q: Can a renderer accept an annual statement of age (such as an affidavit) from a feedlot certifying that dead stock coming from their facility are all under 30 months of age?

A: Nothing in the rule prevents this type of documentation if it meets the requirements in 589.2001(c)(3)(i) (A) or (B).

Removing brain and spinal cord from dead stock cattle

36. Q: How will FDA determine that renderers are adequately removing brain and spinal cord, and will FDA have a zero tolerance for central nervous system tissue?

A: FDA has a variety of means for determining whether renderers are in compliance with the requirements in the 2008 rule, including reviewing renderers’ written procedures, and observing the procedures being used while the facility is operating. With respect to adequacy of brain and spinal cord removal, the rule contains no provision allowing residual brain and spinal cord tissue in material from cattle 30 months of age or older. [See 589.2001(c)(2)(ii), 589.2001(c)(3)(i), 589.2001(e)]. Additional information is available in Draft Guidance for Industry #195.

37. Q: What methods are acceptable for removing brain and spinal cord from dead cattle over 30 months of age?

A: The rule does not specify what method or methods may be used. [See Comment 18]. Additional information about methods of removing the brain and spinal cord can be found in Draft Guidance for Industry #195.

38. Q: Does the definition of CMPAF include the dorsal root ganglia?

A: No.

39. Q: Can the vertebral column be rendered for animal feed use if the spinal cord is removed?

A: Yes. [See Comment 31]

40. Q: Can renderers that harvest skeletal muscle and hides from dead cattle (4-D operations) continue to remove skeletal muscle from cattle carcasses to supply to mink farms and/or greyhound kennels?

A: Yes. Skeletal muscle contains no CMPAF and therefore could be removed from the carcass and used in feed for non-ruminant animals, including food for pets or mink. However, under the rule 4-D operations meet the definition of a renderer and are therefore required to ensure that CMPAF from the remainder of the carcass is properly excluded from animal feed. Such operations are also required to have written procedures in place describing the processes they use to comply with the rule. [See Comment 30]

41. Q: What does “or otherwise effectively excluded from animal feed” mean?

A: The phrase was intended to describe operations where the animal feed (e.g., skeletal muscle for pets or mink) is removed from the CMPAF (i.e. the remainder of the carcass containing the brain and spinal cord), as opposed to operations that remove the CMPAF (brain and spinal cord) so that the remaining material may be used in animal feed. “Removal of brain and spinal cord” does not accurately describe the first type of operation. [See 589.2001(c)(2)(ii) and comments 30 and 40.]

42. Q: Can renderers collect offal from 4-D operations and other renderers?

A: Yes. Both parties would have the same obligations to ensure that CMPAF is excluded from animal feed. [See Comments 30 and 57]

Dedicated equipment/transportation

43. Q: Can the same receiving and processing equipment be used for CMPAF and non-CMPAF materials?

A: No. The rule requires the use of either separate equipment or separate containers for CMPAF that has been separated from non-CMPAF materials. [See 589.2001(c)(2)(iii)(A) & (B)]

44. Q: On a truck, do dead cattle over 30 months of age have to be physically separated from dead cattle under 30 months of age?

A: No. The rule only requires separate equipment or containers once the CMPAF has been separated from non-CMPAF.

45. Q: Can CMPAF be hauled on the same truck as slaughter offal intended to be used in animal feed if it is in a separate container or compartment?

A: Yes, provided there is no cross-contamination between containers or compartments.

Tallow

Table1

Source of Tallow Insoluble Impurities Level

Feed Use Caution Statement Required Regulation

any source (non-CMPAF or CMPAF) < or =" 0.15%" href="mhtml:%7B33B38F65-8D2E-434D-8F9B-8BDCD77D3066%7Dmid://00000038/!x-usc:http://www.aocs.org/">http://www.aocs.org/
), or viewed at the FDA Center for Food Safety and Applied Nutrition’s Library or at the National Archives and Records Administration. [See 589.2001(b)(1)(vi)(B)]

54. Q: What is the analytical variation (AV) for samples analyzed using the AOCS method? AAFCO does not list an acceptable analytical variation (AV) for insoluble impurities. Will acceptable variation for comparing results from different labs be developed? Will FDA verify suitability of labs, methods used, and results?

A: FDA has not established an AV for this analytical method. FDA welcomes any information indicating that variation in test results is presenting difficulties in establishing that tallow meets the impurity standard. Firms using methods other than the AOCS method must have data or other information showing that the method is equivalent in accuracy, precision, and sensitivity to the AOCS method.

55. Q: If a facility receives a load of tallow that is labeled with the “do not feed to cattle or other ruminants” caution statement, but then tests it and find that it contains 0.15% or less insoluble impurities, can the facility use this tallow in ruminant feed?

A: No. While the impurities may settle out to the point where the tallow meets the standard, we do not believe that this is a reliable approach for facilities to use to comply with the requirements of the regulation. We therefore expect the caution statement on the label to be followed.

56. Q: Is there an insoluble impurities standard for blended fats/oils?

A: FDA regulations do not establish a standard for insoluble impurities in any other types of fats or oils except tallow (animal fat from cattle). However, some of the ingredient definitions adopted by the Association of American Feed Control Officials (AAFCO) do establish a maximum amount of insoluble impurities that may be present in a product. Tallow that is to be blended with other fats/oils for use in cattle feed must meet the 0.15% insoluble impurities standard before it is blended. Blending or dilution may not be used to meet the insoluble impurities standard.

57. Q: Does a renderer need to supply a Certificate of Analysis (COA) for every load of tallow delivered to a customer?

A: The regulation does not require that a certificate of analysis accompany every load of tallow. A label must accompany every load, however. The AAFCO ingredient definition for “animal fat” contains more specific information on how tallow is to be labeled.

Import and Export of Animal Proteins

58. Q: Are animal proteins being imported into the US from other countries required to have CMPAF removed?

A: Yes, unless the exporting country has been designated as exempt from the requirement. The rule contains a provision allowing countries to apply for such an exemption. Any country seeking such a designation would have to provide sufficient scientific evidence to support its claimed BSE risk status. [See 589.2001(b)(1)(vi)(C) and 589.2001(f)]

59. Q: Will CMPAF removal also be required for ruminant protein meals destined for export?

A: Feed containing CMPAF intended for export is not deemed to be adulterated or misbranded if it complies with the requirements of section 801(e)(1) of the Federal Food, Drug, and Cosmetic Act.

Compliance

60. Q: What are the consequences for failure in age determination or brain/spinal cord removal?

A: FDA’s enforcement response for failing to comply with this rule will be consistent with enforcement responses used for non-compliance with other FDA regulations. These consequences could include opportunity to make immediate correction, warning letter, seizure, injunction and criminal penalties.

61. Q: Will FDA continue to use the designations NAI, VAI and OAI to categorize renderer compliance with the new rule?

A: Yes.

Recall

62. Q: Will a recall be required if it is determined that a renderer did not properly remove brain and spinal cord from dead cattle, or a slaughter establishment did not properly segregate CMPAF from slaughter offal, even if all parties involved made good faith efforts to comply?

A: Decisions to require recalls will be determined on a case-by-case basis, as the Agency does with all other regulated products.

63. Q: Would recalls concerning CMPAF be Class II or Class III?

A: Classification of a recall depends on the circumstances of an individual case.

Records

64. Q: How long are records required to be kept?

A: The rule requires that records be kept for one year. [See 589.2001(e)]

65. Q: Are electronic records acceptable for meeting the one year record-keeping requirement, or is it necessary to maintain the original documents?

A: Documents may be stored electronically. However, as with hard copies, electronic records must still be made available for inspection and copying, if necessary, at the time and location of the inspection.

66. Q: What does “track CMPAF to ensure the materials are not introduced into animal feed” mean? Are renderers responsible beyond giving up control of the material?

A: The renderer is responsible for marking the CMPAF and disposing of it directly, or arranging for its non-feed disposal. See Draft Guidance for Industry #195 for further details.

Marking

67. Q: What are the marking requirements in the new rule?

A: The rule requires that once CMPAF has been separated from other cattle materials, renderers mark CMPAF with an agent that can be readily detected on visual inspection. This requirement is intended to prevent cross-contamination, and as explained in the preamble to the 2008 rule, is also intended to provide a readily detectable method by which all persons in the animal feed chain can be made aware that the product is prohibited material or contains prohibited material. [See Requirements B(1) page 22735]

68. Q: If CMPAF is rendered to obtain tallow, shouldn’t the finished meal be marked/dyed rather than the raw CMPAF? Marking the raw CMPAF will cause the tallow to be marked as CMPAF when, if it contains less than 0.15% insoluble impurities, it is not CMPAF.

A: The marking requirement has been addressed in more detail in Draft Guidance for Industry #195.

Cleanout of equipment at feed manufacturing facilities

69. Q: Do feed mills have to clean out their tallow tanks before April 27, 2009?

A: Although the rule does not require tallow tanks to be cleaned out prior to the April 27, 2009 effective date, tallow must meet the new requirements that go into effect on that date. Whether this is accomplished through physical cleaning, by switching to new product that complies with the 2008 revision to 21 CFR 589.2000 in advance of the effective date, or by some other means, the method used for bringing tallow tanks into compliance should be documented to meet the record keeping requirement of the new rule.

70. Q: Do feed mills need to steam-clean or power-wash the inside of their tallow tanks before putting in new product that complies with the 0.15% insoluble impurities standard?

A: As stated above, the rule does not require tallow tanks to be cleaned prior to the April 27, 2009 effective date, However, as mentioned above, physical cleaning such as steam-cleaning or power-washing the inside of the tanks prior to putting new product into the tanks may be one way of bringing tallow tanks into compliance. If such cleaning is performed, the date and method should be recorded to meet the recordkeeping requirements of the rule to demonstrate compliance.

71. Q: If a feed mill uses tallow that exceeds the 0.15% insoluble impurities standard to make swine or poultry feeds, but wants to make ruminant feed that doesn’t contain tallow, is cleanout of the mixer or other manufacturing equipment required?

A: Tallow (from non-CMPAF material) that exceeds 0.15% insoluble impurities is now considered “prohibited material” and subject to cleanout requirements under 21 CFR 589.2000. Therefore, if common equipment is used to receive tallow that exceeds 0.15% insoluble impurities and ingredients that may be used in ruminant feeds, then facilities should adopt cleanout procedures for that equipment. However, we expect that it may be possible to minimize the amount of tallow carried-over in the mixing equipment and downstream from the mixer. Therefore, extra cleanout procedures may not be needed if other procedures are in place to address carry over.



http://www.fda.gov/cvm/bse_QA.htm



[Docket No. FSIS-2008-0022] RIN [0583-AD35] Requirements for the Disposition of Cattle that Become Non-Ambulatory Disabled Following Ante-Mortem Inspection



http://www.fsis.usda.gov/oppde/rdad/FRPubs/2008-0022F.pdf



Saturday, February 21, 2009 Renderers say industry not prepared for FDA feed ban rule ??? WHAT, IT'S 2009 FOR PETE'S SAKE $$$ Two recent articles caught my eye ;

Renderers say industry not prepared for FDA feed ban rule

Food Chemical News

February 2, 2009

and

BSE, rendering relate to human safety

Emma Struve 02/17/2009



http://madcowfeed.blogspot.com/2009/02/renderers-say-industry-not-prepared-for.html



Risk of Introduction of BSE into Japan by the Historical Importation of Live Cattle from the United Kingdom (USA AND CANADA)



http://bseusa.blogspot.com/2009/03/risk-of-introduction-of-bse-into-japan.html



Wednesday, January 28, 2009

TAFS1 Position Paper on Specified Risk Materials (January, 2009)

TAFS INTERNATIONAL FORUM FOR TRANSMISSIBLE ANIMAL DISEASES AND FOOD SAFETY a non-profit Swiss Foundation

(January 2009)

TAFS1 Position Paper on Specified Risk Materials



http://madcowspontaneousnot.blogspot.com/2009/01/tafs1-position-paper-on-specified-risk.html



TAFS1 Position Paper on Testing of Cattle for BSE (Revision January 2009)



http://madcowtesting.blogspot.com/2009/02/tafs1-position-paper-on-testing-of.html



Wednesday, February 11, 2009 Atypical BSE North America Update February 2009



http://bse-atypical.blogspot.com/2009/02/atypical-bse-north-america-update.html



10,000,000+ LBS. of PROHIBITED BANNED MAD COW FEED I.E. BLOOD LACED MBM IN COMMERCE USA 2007

Date: March 21, 2007 at 2:27 pm PST

RECALLS AND FIELD CORRECTIONS: VETERINARY MEDICINES -- CLASS II

___________________________________

PRODUCT

Bulk cattle feed made with recalled Darling's 85% Blood Meal, Flash Dried, Recall # V-024-2007

CODE

Cattle feed delivered between 01/12/2007 and 01/26/2007

RECALLING FIRM/MANUFACTURER

Pfeiffer, Arno, Inc, Greenbush, WI. by conversation on February 5, 2007.

Firm initiated recall is ongoing.

REASON

Blood meal used to make cattle feed was recalled because it was cross-contaminated with prohibited bovine meat and bone meal that had been manufactured on common equipment and labeling did not bear cautionary BSE statement.

VOLUME OF PRODUCT IN COMMERCE

42,090 lbs.

DISTRIBUTION

WI

___________________________________

PRODUCT

Custom dairy premix products: MNM ALL PURPOSE Pellet, HILLSIDE/CDL Prot-Buffer Meal, LEE, M.-CLOSE UP PX Pellet, HIGH DESERT/ GHC LACT Meal, TATARKA, M CUST PROT Meal, SUNRIDGE/CDL PROTEIN Blend, LOURENZO, K PVM DAIRY Meal, DOUBLE B DAIRY/GHC LAC Mineral, WEST PIONT/GHC CLOSEUP Mineral, WEST POINT/GHC LACT Meal, JENKS, J/COMPASS PROTEIN Meal, COPPINI - 8# SPECIAL DAIRY Mix, GULICK, L-LACT Meal (Bulk), TRIPLE J - PROTEIN/LACTATION, ROCK CREEK/GHC MILK Mineral, BETTENCOURT/GHC S.SIDE MK-MN, BETTENCOURT #1/GHC MILK MINR, V&C DAIRY/GHC LACT Meal, VEENSTRA, F/GHC LACT Meal, SMUTNY, A-BYPASS ML W/SMARTA, Recall # V-025-2007

CODE

The firm does not utilize a code - only shipping documentation with commodity and weights identified.

RECALLING FIRM/MANUFACTURER

Rangen, Inc, Buhl, ID, by letters on February 13 and 14, 2007. Firm initiated recall is complete.

REASON

Products manufactured from bulk feed containing blood meal that was cross contaminated with prohibited meat and bone meal and the labeling did not bear cautionary BSE statement.

VOLUME OF PRODUCT IN COMMERCE

9,997,976 lbs.

DISTRIBUTION

ID and NV

END OF ENFORCEMENT REPORT FOR MARCH 21, 2007



http://www.fda.gov/bbs/topics/enforce/2007/ENF00996.html



Friday, November 21, 2008

Plasma & Serum Proteins Receive Continued FDA Approval



http://madcowfeed.blogspot.com/2008/11/plasma-serum-proteins-receive-continued.html



http://madcowfeed.blogspot.com/



Thursday, November 27, 2008 Prion diseases are efficiently transmitted by blood transfusion in sheep



http://vcjdblood.blogspot.com/2008/11/prion-diseases-are-efficiently.html



Scientists warn of first ever case of human mad cow disease from blood plasma



http://vcjdtransfusion.blogspot.com/2009/02/scientists-warn-of-first-ever-case-of.html



November 25, 2008

Update On Feed Enforcement Activities To Limit The Spread Of BSE



http://madcowfeed.blogspot.com/2008/11/november-2008-update-on-feed.html



Docket APHIS-2007-0033 Docket Title Agricultural Bioterrorism Protection Act of 2002; Biennial Review and Republication of the Select Agent and Toxin List Docket Type Rulemaking Document APHIS-2007-0033-0001 Document Title Agricultural Bioterrorism Protection Act of 2002; Biennial Review and Republication of the Select Agent and Toxin List Public Submission APHIS-2007-0033-0002.1 Public Submission Title Attachment to Singeltary comment



http://www.regulations.gov/fdmspublic/component/main?main=DocumentDetail&o=090000648027c28e



Manuscript Draft Manuscript Number: Title: HUMAN and ANIMAL TSE Classifications i.e. mad cow disease and the UKBSEnvCJD only theory Article Type: Personal View Corresponding Author: Mr. Terry S. Singeltary, Corresponding Author's Institution: na First Author: Terry S Singeltary, none Order of Authors: Terry S Singeltary, none; Terry S. Singeltary Abstract: TSEs have been rampant in the USA for decades in many species, and they all have been rendered and fed back to animals for human/animal consumption. I propose that the current diagnostic criteria for human TSEs only enhances and helps the spreading of human TSE from the continued belief of the UKBSEnvCJD only theory in 2007.



http://www.regulations.gov/fdmspublic/ContentViewer?objectId=090000648027c28e&disposition=attachment&contentType=pdf




Docket APHIS-2006-0041 Docket Title Bovine Spongiform Encephalopathy; Minimal-Risk Regions; Importation of Live Bovines and Products Derived from Bovines Commodities Docket Type Rulemaking Document APHIS-2006-0041-0001 Document Title Bovine Spongiform Encephalopathy; Minimal-Risk Regions; Importation of Live Bovines and Products Derived From Bovines Public Submission APHIS-2006-0041-0028 Public Submission Title Comment from Terry S Singletary

Comment 2006-2007 USA AND OIE POISONING GLOBE WITH BSE MRR POLICY

THE USA is in a most unique situation, one of unknown circumstances with human and animal TSE. THE USA has the most documented TSE in different species to date, with substrains growing in those species (BSE/BASE in cattle and CWD in deer and elk, there is evidence here with different strains), and we know that sheep scrapie has over 20 strains of the typical scrapie with atypical scrapie documented and also BSE is very likely to have passed to sheep. all of which have been rendered and fed back to animals for human and animal consumption, a frightening scenario. WE do not know the outcome, and to play with human life around the globe with the very likely TSE tainted products from the USA, in my opinion is like playing Russian roulette, of long duration, with potential long and enduring consequences, of which once done, cannot be undone. These are the facts as I have come to know through daily and extensive research of TSE over 9 years, since 12/14/97. I do not pretend to have all the answers, but i do know to continue to believe in the ukbsenvcjd only theory of transmission to humans of only this one strain from only this one TSE from only this one part of the globe, will only lead to further failures, and needless exposure to humans from all strains of TSE, and possibly many more needless deaths from TSE via a multitude of proven routes and sources via many studies with primates and rodents and other species.

MY personal belief, since you ask, is that not only the Canadian border, but the USA border, and the Mexican border should be sealed up tighter than a drum for exporting there TSE tainted products, until a validated, 100% sensitive test is available, and all animals for human and animal consumption are tested. all we are doing is the exact same thing the UK did with there mad cow poisoning when they exported it all over the globe, all the while knowing what they were doing. this BSE MRR policy is nothing more than a legal tool to do just exactly what the UK did, thanks to the OIE and GW, it's legal now. and they executed Saddam for poisoning ???

go figure. ...



http://www.regulations.gov/fdmspublic/component/main?main=DocumentDetail&o=09000064801f8151




Docket Management Docket: 02N-0273 - Substances Prohibited From Use in

Animal Food or Feed; Animal Proteins Prohibited in Ruminant Feed

Comment Number: EC -10

Accepted - Volume 2



http://www.fda.gov/ohrms/dockets/dailys/03/Jan03/012403/8004be07.html



PART 2



http://www.fda.gov/ohrms/dockets/dailys/03/Jan03/012403/8004be09.html




TSS