Data Foundry

Drug recalls 2015

Hydrochlorothiazide Tablet USP 25 mg — Class II drug recall D-1352-2015

Terminated recall by Unichem Pharmaceuticals Usa Inc, reported 2015-09-02, distributed nationwide. Presence of Foreign Tablet: A pharmacist found a clopidogrel tablet in the 1000-count bottle of hydrochlorothi

Recall numberD-1352-2015
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmUnichem Pharmaceuticals Usa Inc, Rochelle Park, NJ, United States
Recall initiated2015-07-30
Classified2015-08-25
Reported by FDA2015-09-02
Terminated2018-10-19
DistributedNationwide (US)
Quantity4,776 bottles
NDC29300-0128, 29300-0128-01, 29300-0128-05, 29300-0128-10, 29300-0128-50, 29300-0129, 29300-0129-01, 29300-0129-05, 29300-0129-10, 29300-0129-50, 29300-0485, 29300-0485-01, 29300-0485-10
Lot numbersGHYL15028
Expiration dates2018-04-20

Product

Hydrochlorothiazide Tablet USP 25 mg,1000- count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Marketed by: UNICHEM PHARMACEUTICALS (USA), INC. Rochelle Park, NJ 07662, NDC 29300-128-10

Reason for recall

Presence of Foreign Tablet: A pharmacist found a clopidogrel tablet in the 1000-count bottle of hydrochlorothiazide 25 mg tablets.

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-1352-2015. 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.