Data Foundry

Drug recalls 2026

Doxazosin Tablets — Class III drug recall D-0306-2026

Ongoing recall by Unichem Pharmaceuticals USA Inc., reported 2026-02-18, distributed nationwide. Tablets/Capsules Imprinted with Wrong ID

Recall numberD-0306-2026
Product typeDrug
ClassificationClass III
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmUnichem Pharmaceuticals USA Inc., East Brunswick, NJ, United States
Recall initiated2026-01-21
Classified2026-02-11
Reported by FDA2026-02-18
DistributedNationwide (US)
Quantity60,000 tablets
NDC29300-0351, 29300-0351-01, 29300-0351-10, 29300-0351-13, 29300-0352, 29300-0352-01, 29300-0352-10, 29300-0352-13, 29300-0353, 29300-0353-01, 29300-0353-10, 29300-0353-13, 29300-0354, 29300-0354-01, 29300-0354-10, 29300-0354-13
Lot numbersGDSH25006
Expiration dates2027-08

Product

Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10.

Reason for recall

Tablets/Capsules Imprinted with Wrong ID

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0306-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.