Recalls / Class I
Class ID-0302-2024
Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.
Product
Velocity Pharma brand Lubricating Eye Drop (Propylene glycol Eye Drops 0.6%), packaged in 3 bottles of 0.33 FL OZ (10 mL) each, Velocity Pharma, NDC 76168-502-30
- Affected lot / code info
- All lots
Why it was recalled
Non-Sterility
Recalling firm
- Firm
- Kilitch Healthcare India Limited
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- R - 904 905 T T C Industrial Road, Navi Mumbai, N/A, India
Distribution
- Quantity
- 2,820 bottles
- Distribution pattern
- Nationwide within the United States
Timeline
- Recall initiated
- 2023-11-13
- FDA classified
- 2024-02-05
- Posted by FDA
- 2024-02-14
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0302-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.