FDA Drug Recalls

Recalls / Class II

Class IID-0513-2023

Product

Clopidogrel Tablets USP, 75 mg, 90-count bottles, Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703, NDC 68788-8190-9

Affected lot / code info
Lot: E0922W, G1222E, I0922W and K3022W Exp 10/31/2023.

Why it was recalled

cGMP Deviations for the manufacturing Firm (Accord Healthcare) after their inspection.

Recalling firm

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

Distribution

Quantity
72 Bottles
Distribution pattern
USA Nationwide

Timeline

Recall initiated
2023-03-23
FDA classified
2023-04-06
Posted by FDA
2023-04-12
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0513-2023. 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