US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 30, 2015 (11 years ago)

Hydrochlorothiazide Tablet USP 25 mg,1000- count bottle, Rx Only, Manufactured by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Unichem Pharmaceuticals Usa Inc
NDC code
29300-128-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1352-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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