Safety
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Industry Guidance
Information on Recalls of FDA Regulated Products
Last Update: 12-14-2011
- Industry Recall Guidance: Product Recalls, Including Removals and Corrections
- Recalls Background and Definitions
- Recall Regulations in 21 CFR Part 7
- Index of Model Press Releases:
- Allergens (Allergy Alert)
- Listeria monocytogenes
- Clostridium botulinum
- Salmonella (all serotypes)
- E. coli 0157:H7
- Medical Device
- Human Drug
- District Recall Coordinators
- Index of Generic Model Letter Exhibits in FDA Regulatory Procedures Manual:
- Medical Device Model Recall Notification Letter and Response Form
- Medical Device Recall Training Modules
- Assisting Interested Parties in Addressing Marketplace Confusion Over the Identity of Food Products Subject to Recall
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