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Class II · ModerateActive recall

Carbamazepine

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: a) GS067429, GS068091, Exp 5/31/2028; b) GS067430, GS068090, Exp 5/31/2028
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP deviations: tablets with black specks.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byTaro Pharmaceutical Industries Ltd., Marketed by: GSMS, Incorporated, Camarillo, CA 93012 USA
Brand nameCARBAMAZEPINE
Generic nameCARBAMAZEPINE
Active ingredient(s)CARBAMAZEPINE
Distributed by / forGolden State Medical Supply Inc.
NDC51407-215-10
Show the full FDA record
Full product labelCarbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count bottles (NDC 51407-215-01), Rx Only, Manufactured by: Taro Pharmaceutical Industries Ltd., Marketed by: GSMS, Incorporated, Camarillo, CA 93012 USA
Recalling firmGolden State Medical Supply Inc.
DistributionUSA Nationwide
Quantity1200 bottles
Recall initiated2026-08-07
Report date2026-08-26
Recall completed
Recall numberD-0771-2026
ClassificationClass II
FDA statusOngoing
Origin on fileCamarillo CA United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.