FDA Drug Recalls

Recalls / Class II

Class IID-0518-2023

Product

Montelukast Sodium Tablets, USP, 10 mg, packaged in: a) 30-count bottle (NDC 68788-9438-3); b) 60-count bottle (NDC 68788-9438-6); c) 90-count bottle (NDC 68788-9438-9), Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703.

Affected lot / code info
a) Lot: F3021D, Exp 12/31/2023, Lot: L0722T, Exp 5/31/2025; b) Lot: F1021I, Exp 12/31/2023; c) Lot:H1721R, Exp 12/31/2023, Lot: L0722E, Exp 5/31/2025.

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
a) 266 Bottles, b) not reported, c) 216 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-0518-2023. 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