RecallRadar

FDA Drug recall D-1114-2018

Camber Pharmaceuticals, Inc

On 2018-08-29 the FDA classified a Class II recall of Camber Pharmaceuticals, Inc by Hetero Labs Unit V, citing CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1114-2018
ClassificationClass II
Statuscompleted
Initiated2018-08-08
Published2018-08-29
Last updated2026-09-13 11:52 UTC
CompanyHetero Labs Unit V
DistributionUS

Product

Camber Pharmaceuticals, Inc. Valsartan Tablets, USP, 80 mg, 90 count bottles, Rx Only Manufactured for: Camber Pharmaceuticals, Inc. Piscataway NJ 08854 By: Hetero Hetero Labs Limited Unit V. Polepally Jadcherla Mahaboob Nagar - 509-301 India. NDC 31722-746-90 UPC 331722746908

Reason

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

Identifiers

upc331722746908
ndc31722-745-30
ndc31722-745-90
ndc31722-745-05
ndc31722-745-31
ndc31722-745-32
ndc31722-746-30
ndc31722-746-90
ndc31722-746-05
ndc31722-746-31
ndc31722-746-32
ndc31722-747-30
ndc31722-747-90
ndc31722-747-05
ndc31722-747-31
ndc31722-747-32
ndc31722-748-30
ndc31722-748-90
ndc31722-748-05
ndc31722-748-31
ndc31722-748-32
ndc3317227469
code_infoAll Lots with expiration dates 7/2018 to 6/2020

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1114-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.