FDA Drug Recalls

Recalls / Class II

Class IID-0391-2025

Product

Clindamycin Hydrochloride Capsules, USP, 300mg, 30-count bottles, Manufactured by: Glenmark Pharmaceuticals Limited, NDC 68788-8685-03.

Affected lot / code info
Lot #: L0224T, K1824M, K0124N, J1624V, J0824O, I2424E, I1024O, A0925F, L2324L, Exp: 7/31/2026.

Why it was recalled

cGMP Deviations

Recalling firm

Firm
Preferred Pharmaceuticals, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1250 N Lakeview Ave Ste O, N/A, Anaheim, California 92807-1801

Distribution

Quantity
1190 Bottles
Distribution pattern
Nationwide in the US

Timeline

Recall initiated
2025-04-18
FDA classified
2025-04-28
Posted by FDA
2025-05-07
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0391-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls