January 12, 2007
January 2007 Update on Feed Enforcement Activities to Limit the Spread of BSE
To help prevent the establishment and amplification of BSE through feed in the
The following information is an update on FDA enforcement activities regarding the ruminant feed ban. FDA's Center for Veterinary Medicine (CVM) has assembled data from the inspections that have been conducted and whose final inspection report has been recorded in the FDA's inspection database as of January 6, 2007. As of January 6, 2007, FDA had received over 50,000 inspection reports. The majority of these inspections (around 68%) were conducted by State feed safety officials, with the remainder conducted by FDA officials.
Inspections conducted by FDA or State investigators are classified to reflect the compliance status at the time of the inspection based upon the objectionable conditions documented. These inspection conclusions are reported as Official Action Indicated (OAI), Voluntary Action Indicated (VAI), or No Action Indicated (NAI).
An OAI inspection classification occurs when significant objectionable conditions or practices were found and regulatory sanctions are warranted in order to address the establishment's lack of compliance with the regulation. An example of an OAI inspection classification would be findings of manufacturing procedures insufficient to ensure that ruminant feed is not contaminated with prohibited material. Inspections classified with OAI violations will be promptly re-inspected following the regulatory sanctions to determine whether adequate corrective actions have been implemented.
A VAI inspection classification occurs when objectionable conditions or practices were found that do not meet the threshold of regulatory significance, but do warrant advisory actions to inform the establishment of findings that should be voluntarily corrected. Inspections classified with VAI violations are more technical violations of the Ruminant Feed Ban. These include provisions such as minor recordkeeping lapses and conditions involving non-ruminant feeds.
An NAI inspection classification occurs when no objectionable conditions or practices were found during the inspection or the significance of the documented objectionable conditions found does not justify further actions.
The results to date are reported here both by “segment of industry” and “in total”. NOTE – A single firm can operate as more than one firm type. As a result, the categories of the different industry segments are not mutually exclusive.
RENDERERS
These firms are the first to handle and process (i.e., render) animal proteins and to send these processed materials to feed mills and/or protein blenders for use as a feed ingredient.
Number of active firms whose initial inspection has been reported to FDA – 271 Number of active firms handling materials prohibited from use in ruminant feed – 169 (62% of those active firms inspected) Of the 169 active firms handling prohibited materials, their most recent inspection revealed that:
- 1 firm (0.6%) was classified as OAI
- 2 firms (1.2%) were classified as VAI
LICENSED FEED MILLS
FDA licenses these feed mills to produce medicated feed products. The license is required to manufacture and distribute feed using certain potent drug products, usually those requiring some pre-slaughter withdrawal time. This licensing has nothing to do with handling prohibited materials under the feed ban regulation. A medicated feed license from FDA is not required to handle materials prohibited under the Ruminant Feed Ban.
Number of active firms whose initial inspection has been reported to FDA – 1,077 Number of active firms handling materials prohibited from use in ruminant feed – 445 (41% of those active firms inspected) Of the 445 active firms handling prohibited materials, their most recent inspection revealed that:
- 1 firm (0.2%) was classified as OAI
- 5 firms (1.1%) were classified as VAI
FEED MILLS NOT LICENSED BY FDA
These feed mills are not licensed by the FDA to produce medicated feeds.
Number of active firms whose initial inspection has been reported to FDA – 5,211 Number of active firms handling materials prohibited from use in ruminant feed – 2,360 (45% of those active firms inspected) Of the 2,360 active firms handling prohibited materials, their most recent inspection revealed that:
- 3 firms (0.1%) were classified as OAI
- 48 firms (2.0%) were classified as VAI
PROTEIN BLENDERS
These firms blend rendered animal protein for the purpose of producing quality feed ingredients that will be used by feed mills.
Number of active firms whose initial inspection has been reported to FDA -- 362 Number of active firms handling materials prohibited from use in ruminant feed – 187 (52% of those active firms inspected) Of the 187 active firms handling prohibited materials, their most recent inspection revealed that:
- 2 firms (1.1%) were classified as OAI
- 2 firms (1.1%) were classified as VAI
RENDERERS, FEED MILLS, AND PROTEIN BLENDERS MANUFACTURING WITH PROHIBITED MATERIAL
This category includes only those firms that actually use prohibited material to manufacture, process, or blend animal feed or feed ingredients.
Total number of active renderers, feed mills, and protein blenders whose initial inspection has been reported to FDA – 6,636 Number of active renderers, feed mills, and protein blenders processing with prohibited materials – 497 (7.5%) Of the 497 active renderers, feed mills, and protein blenders processing with prohibited materials, their most recent inspection revealed that:
- 6 firms (1.2%) were classified as OAI
- 16 firms (3.2%) were classified as VAI
OTHER FIRMS INSPECTED
Examples of such firms include ruminant feeders, on-farm mixers, pet food manufacturers, animal feed salvagers, distributors, retailers, and animal feed transporters.
Number of active firms whose initial inspection has been reported to FDA – 16,653 Number of active firms handling materials prohibited from use in ruminant feed – 5,227 (31% of those active firms inspected) Of the 5,227 active firms handling prohibited materials, their most recent inspection revealed that:
- 4 firms (0.1%) were classified as OAI
- 178 firms (3.4%) were classified as VAI
TOTAL FIRMS
Note that a single firm can be reported under more than one firm category; therefore, the summation of the individual OAI/VAI firm categories will be more than the actual total number of OAI/VAI firms, as presented below.
Number of active firms whose initial inspection has been reported to FDA – 19,492 Number of active firms handling materials prohibited from use in ruminant feed – 5,905 (30% of those active firms inspected) Of the 5,905 active firms handling prohibited materials, their most recent inspection revealed that:
- 7 firms (0.1%) were classified as OAI
- 188 firms (3.2%) were classified as VAI
Issued by:
FDA, Center for Veterinary Medicine,
Communications Staff, HFV-12
7519 Standish Place, Rockville, MD 20855
Telephone: (240) 276-9300 FAX: (240) 276-9115
Internet Web Site: http://www.fda.gov/cvm
|
||||||
 |
||||||
|
||||||