RecallRadar

FDA Drug recall D-0140-2020

Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ, Manuf…

On 2019-10-23 the FDA classified a Class II recall of Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ, Manuf… by Macleods Pharma Usa, citing superpotent.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0140-2020
ClassificationClass II
Statusterminated
Initiated2019-09-23
Published2019-10-23
Last updated2026-09-13 11:52 UTC
CompanyMacleods Pharma Usa
Distributionn/a

Product

Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, India NDC 33342-054-07

Reason

Superpotent

Identifiers

ndc33342-054-07
ndc33342-054-10
ndc33342-054-15
ndc33342-054-12
ndc33342-055-07
ndc33342-055-10
ndc33342-055-15
ndc33342-055-12
ndc33342-056-07
ndc33342-056-10
ndc33342-056-15
ndc33342-056-12
code_infoLot # BPF901A, exp. date 12/2021

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-0140-2020%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.