RecallRadar

FDA Drug recall D-1164-2022

Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC # 33342-052-…

On 2022-07-06 the FDA classified a Class II recall of Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC # 33342-052-… by Macleods Pharma Usa, citing CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1164-2022
ClassificationClass II
Statusterminated
Initiated2022-06-10
Published2022-07-06
Last updated2026-09-13 11:52 UTC
CompanyMacleods Pharma Usa
DistributionUS

Product

Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg, 30, 90 & 1000 count NDC # 33342-052-07, NDC #33342-052-10 & NDC # 33342-052-44, Rx Only, MFR: Macleods Pharma USA, Inc. Plainsboro, NJ 08536

Reason

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

Identifiers

ndc33342-050-07
ndc33342-050-10
ndc33342-050-44
ndc33342-050-12
ndc33342-051-07
ndc33342-051-10
ndc33342-051-44
ndc33342-051-12
ndc33342-052-07
ndc33342-052-10
ndc33342-052-44
ndc33342-052-12
code_infoLot # BLM2114A, exp. date 07/2023

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1164-2022%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.