Product Recalls

Product Recalls

Company
Product

Document Type Product Recalls - Class I or II (Severe or Moderate Severity Potential)
Product Recalls - Class III (Minor Consequences to Health)
Medical Device Reports - Death or Serious Injury
Medical Device Reports - Malfunctions
All Document Types

Category
Date

Help? E-Mail help desk

Company
Product
Document Type	Product Recalls - Class I or II (Severe or Moderate Severity Potential) Product Recalls - Class III (Minor Consequences to Health) Medical Device Reports - Death or Serious Injury Medical Device Reports - Malfunctions All Document Types
Category
Date

	E-Mail help desk

Search Tips
Choose Your Options
Use only the search options that you need--leave the others blank.
Company
Enter the name of a company. Leave out words like Corp., Inc., Ltd, etc. You can search for multiple companies. For example, BAUSCH & LOMB OR BIOVISION.
Product
Enter words that must appear in the name of the product or device. You can use the wildcard and combine words. For example: LASER? AND SURGER?

Sources
DIOGENES® FDA Regulatory Updates covers reports on product recalls, safety alerts, product seizures, field corrections, related enforcement actions, and Medical Device Reports (MDRs) published by the U.S. FDA (Food and Drug Administration).