FDA Drug Recalls

Recalls / Class I

Class ID-0307-2024

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

Lubricant Gel Drops (Polyethylene glycol 400 0.4%, Propylene glycol 0.3%), packaged in 0.33 FL OZ (10 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4540-3

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
7,776 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-0307-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.