Tizanidine: 8 recalls on record

Recalled by 1 agency: FDA (8).

First recall on record: April 10, 2013. Most recent: January 17, 2024.

Risk classification: Class II: 7 · Class III: 1

Most recent recalls

DateAgencyProduct
January 17, 2024FDATizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories…D-0223-2024
July 26, 2023FDATizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Lab…D-0923-2023
July 12, 2023FDATizanidine Tablets, USP, 4 mg, 100 Tablets (10 tablets x 10 unit dose blister packs) per …D-0892-2023
July 12, 2023FDATizanidine Hydrochloride Tablet 4mg, packaged in a) 20 count-bottles (NDC 68788-7781-2), …D-0894-2023
August 25, 2021FDATizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laborat…D-0750-2021
December 9, 2020FDATizanidine Tablets, USP 4mg, Rx Only, 150 Tablets per Bottle, Manufactured by Alkem Labor…D-0173-2021
September 26, 2018FDATizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laborat…D-1191-2018
April 10, 2013FDATizanidine Tablets USP, 4 mg, 150-count tablets per bottle, Rx Only, Mfd. By: Dr. Reddy's…D-238-2013

Questions about this brand

How many recalls does Tizanidine have?
Recalert has 8 U.S. recalls on record for Tizanidine, published between April 10, 2013 and January 17, 2024.
What was the most recent Tizanidine recall?
FDA recall D-0223-2024, published January 17, 2024: Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-180-15
Which agencies have recalled Tizanidine products?
Tizanidine products appear in recalls from: FDA (8).

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