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Class II: temporary or reversible health riskTerminated

Dr. Reddy's Laboratories Tizanidine HCl Tablets Recall

Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr

Dr. Reddy's Laboratories, Inc. · Princeton, NJ

Risk level
Class II
Reported by FDA
Aug 25, 2021
Recall ID
D-0750-2021
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Tizanidine HCl Tablets starting Jul 19, 2021. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0750-2021 on Aug 25, 2021. Reason: Failed Tablet/Capsule Specification: Some tablets are shaved. Status: Terminated.

Why it was recalled

Failed Tablet/Capsule Specification: Some tablets are shaved

Product description

Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laboratories limited, Srikakulam District, 532 409 INDIA, NDC 55111-180-15.

Lot numbers, UPCs & expiration codes

Lot #: T2000471, exp date 09/2023

Where it was sold

Nationwide within the United States

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0750-2021
Classification
Class II
Status
Terminated
Recall initiated
Jul 19, 2021
FDA report date
Aug 25, 2021
Quantity
37560 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-0750-2021, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Terminated
Country
United States
Event ID
88309
Address
107 College Rd E
Code information
Lot #: T2000471, exp date 09/2023
Postal code
08540-6623
Report date
Aug 25, 2021
Product type
Drugs
Recall number
D-0750-2021
Classification
Class II
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
37560 bottles
Termination date
Dec 21, 2022
Reason for recall
Failed Tablet/Capsule Specification: Some tablets are shaved
Voluntary / mandated
Voluntary: Firm initiated
Product description
Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laboratories limited, Srikakulam District, 532 409 INDIA, NDC 55111-180-15.
Distribution pattern
Nationwide within the United States
Recall initiation date
Jul 19, 2021
Initial firm notification
Letter
Center classification date
Aug 18, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0750-2021, published Aug 25, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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