RecallRadar

FDA Drug recall D-1191-2018

Tizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd

On 2018-09-26 the FDA classified a Class II recall of Tizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd by Dr Reddy S Laboratories, citing presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a bottle of Tinzadine Hcl Tablets .

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1191-2018
ClassificationClass II
Statusterminated
Initiated2018-09-04
Published2018-09-26
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Tizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited Srilakulam - 532 409 INDIA, NDC 55111-179-15, UPC 35511179153

Reason

Presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a bottle of Tinzadine Hcl Tablets .

Identifiers

ndc55111-179-30
ndc55111-179-15
ndc55111-179-03
ndc55111-179-10
ndc55111-180-30
ndc55111-180-15
ndc55111-180-03
ndc55111-180-10
ndc3551117915
code_infoLot #: T800304, Exp. 03/2021

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-1191-2018%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.