FDA Drug Recalls

Recalls / Class II

Class IID-0318-2020

Product

Equate Maximum Strength Ranitidine Tablets, USP 150 mg Acid Reducer Cool Mint Tablets Sugar Free 65 Tablets NDC: 49035-117-06 Distributed By: Wal-Mart Stores, Inc. Bentonville, AR 72716

Affected lot / code info
All lots remaining within expiry.

Why it was recalled

GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

Recalling firm

Firm
Apotex Inc.
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
150 Signet Drive, N/A, North York, N/A N/A, Canada

Distribution

Quantity
162,344 bottles
Distribution pattern
Nationwide

Timeline

Recall initiated
2019-09-24
FDA classified
2019-11-12
Posted by FDA
2019-11-20
Status
Completed

Source: openFDA Drug Enforcement endpoint. Recall record D-0318-2020. 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