RecallRadar

FDA Drug recall D-0770-2026

Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 262…

On 2026-08-26 the FDA classified a Class II recall of Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 262… by Sun Pharmaceutical Industries, citing CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0770-2026
ClassificationClass II
Statusongoing
Initiated2026-08-03
Published2026-08-26
Last updated2026-09-13 11:52 UTC
CompanySun Pharmaceutical Industries
DistributionUS

Product

Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Distributed by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC 51672-4005-3.

Reason

CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing

Identifiers

ndc51672-4041-1
ndc51672-4041-2
ndc51672-4041-9
ndc51672-4041-0
ndc51672-4050-1
ndc51672-4005-1
ndc51672-4005-2
ndc51672-4005-3
ndc51672-4123-6
ndc51672-4123-1
ndc51672-4123-3
ndc51672-4124-6
ndc51672-4124-1
ndc51672-4124-3
ndc51672-4125-6
ndc51672-4125-1
ndc51672-4125-3
ndc51672-4047-9
ndc51672-4047-4
code_infoLot # AD94033, Exp Date: 5/31/2028.

Status history

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

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0770-2026%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.