🔍 RecallPedia

Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Srikakulam - 532 409 India. NDC 55111-180-10

Class I - Dangerous
💊 Drugs Recalled: June 21, 2023 Dr Reddy's Laboratories Limited Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot: T2100585, T2100586, T2100587, Exp 12/2023
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Dr Reddy's Laboratories Limited
Reason for Recall:
Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Srikakulam - 532 409 India. NDC 55111-180-10

Product Codes/Lot Numbers:

Lot: T2100585, T2100586, T2100587, Exp 12/2023

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0923-2023