Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Tizanidine Tablets USP Recalled by Dr. Reddy'S Laboratories Due to Labeling Illegible: There is a possibility that the...

Date: March 19, 2013
Company: Dr. Reddy'S Laboratories
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Dr. Reddy'S Laboratories directly.

Affected Products

Tizanidine Tablets USP, 4 mg, 150-count tablets per bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepally - 500 090 India; NDC 55111-180-15.

Quantity: 117,546 bottles

Why Was This Recalled?

Labeling Illegible: There is a possibility that the bottle labels do not contain the strength of the product as well as other printing details.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Dr. Reddy'S Laboratories

Dr. Reddy'S Laboratories has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report