FDARecall 99562Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing
FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.
Is it yours? Products and codes
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.
- Lot or code
- Lot # AD94033, Exp Date: 5/31/2028.
- FDA recall number
- D-0770-2026
- Quantity
- 1968 Bottles (1000Tablets/Bottle)
Distribution (FDA): US Nationwide.
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- SUN PHARMACEUTICAL INDUSTRIES INC (other notices of this firm)
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.