RecallRadar

FDA Drug recall D-0312-2024

Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd

On 2024-02-14 the FDA classified a Class III recall of Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd by Dr Reddy S Laboratories, citing misprint on tablet.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0312-2024
ClassificationClass III
Statusongoing
Initiated2024-01-18
Published2024-02-14
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01

Reason

Misprint on tablet

Identifiers

ndc55111-320-30
ndc55111-320-01
ndc55111-320-05
ndc55111-320-79
ndc55111-320-78
ndc55111-321-30
ndc55111-321-01
ndc55111-321-05
ndc55111-321-79
ndc55111-321-78
ndc55111-322-30
ndc55111-322-01
ndc55111-322-05
ndc55111-322-79
ndc55111-322-78
code_infoLot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026

Status history

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

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0312-2024%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.