RecallRadar

FDA Drug recall D-1352-2015

Hydrochlorothiazide Tablet USP 25 mg,1000- count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind

On 2015-09-02 the FDA classified a Class II recall of Hydrochlorothiazide Tablet USP 25 mg,1000- count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind by Unichem Pharmaceuticals Usa, citing presence of Foreign Tablet: A pharmacist found a clopidogrel tablet in the 1000-count bottle of hydrochlorothiazide 25 mg tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1352-2015
ClassificationClass II
Statusterminated
Initiated2015-07-30
Published2015-09-02
Last updated2026-09-13 11:51 UTC
CompanyUnichem Pharmaceuticals Usa
DistributionUS

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

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

Identifiers

ndc29300-128-01
ndc29300-128-05
ndc29300-128-10
ndc29300-128-50
ndc29300-129-01
ndc29300-129-05
ndc29300-129-10
ndc29300-129-50
ndc29300-485-01
ndc29300-485-10
code_infoLot #: GHYL15028, Exp April 2018

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1352-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.