RecallDepth
Class II Ongoing

Tizanidine Hydrochloride Tablet 4mg, packaged in a) 20 count-bottles (NDC 68788-7781-2), b)30-count bottles (NDC: 68788-7781-3), c) 60-count bottles, (NDC: 68788-7781-6), d) 90-count bottles (NDC: 68788-7781-9), e) 120-count bottles (NDC: 68788-7781-8), Rx only, Mfg: Dr. Reddy's Laboratories Limited.

This recall is currently active, issued July 12, 2023. It was issued by Preferred Pharmaceuticals, Inc..

Company
Preferred Pharmaceuticals, Inc.
Recall Initiated
June 26, 2023
Posted
July 12, 2023
Recall Number
D-0894-2023
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
541 Bottles
Firm Location
Anaheim, CA, United States
Official Source
View on FDA website ↗

Reason for Recall

Failed Stability Specifications

Distribution

Nationwide within the United States

Lot / Code Info

Lot#: a) H1621S, Exp: 12/31/2023; b) H2321C, Exp: 12/31/2023; c) H0421B, Exp: 12/31/2023; d) H1721E, H1921T, H3121M, Exp: 12/31/2023, e) H2021G, Exp: 12/31/2023

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