FDA Drug Recalls

Recalls / Class II

Class IID-1136-2018

Product

Valsartan Tablets USP, 320mg, 90 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-070-90

Affected lot / code info
Batch: BV48D001, BV48D002

Why it was recalled

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

Recalling firm

Firm
Torrent Pharma Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
150 Allen Rd Ste 102, N/A, Basking Ridge, New Jersey 07920-3856

Distribution

Quantity
ALL
Distribution pattern
Nationwide USA

Timeline

Recall initiated
2018-08-17
FDA classified
2018-08-28
Posted by FDA
2018-09-05
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-1136-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.