FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Tizanidine

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: T2304007, Exp 7/31/2026
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byDr. Reddy's Laboratories Limited
Brand nameTIZANIDINE
Generic nameTIZANIDINE
Active ingredient(s)TIZANIDINE HYDROCHLORIDE
Distributed by / forDr. Reddy's Laboratories, Inc.
NDC55111-180-15
Show the full FDA record
Full product labelTizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-180-15
Recalling firmDr. Reddy's Laboratories, Inc.
DistributionUSA Nationwide
Quantity38,952 bottles
Recall initiated2024-01-02
Report date2024-01-17
Recall completed—
Recall numberD-0223-2024
ClassificationClass II
FDA statusCompleted
Origin on filePrinceton NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.