FDA Drug Recalls

Recalls / Class II

Class IID-1027-2018

Product

Valsartan 80 mg tablets, 90-count bottles (NDC 63629-6922-2), 60-count bottles ( 63629-6922-3), 28-count bottles (63629-6922-4), Rx Only, Packaged by Bryant Ranch, Burbank, CA 91504.

Affected lot / code info
Lot # 111158; Exp. 02/19

Why it was recalled

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Recalling firm

Firm
Bryant Ranch Prepack Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1919 N Victory Pl, N/A, Burbank, California 91504-3425

Distribution

Quantity
690 tablets
Distribution pattern
Product was distributed in HI, IN, and FL.

Timeline

Recall initiated
2018-07-27
FDA classified
2018-08-02
Posted by FDA
2018-08-08
Terminated
2021-04-22
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1027-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.