PlainRecalls
FDA Drug Critical Class I Completed

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

Reported: November 10, 2021 Initiated: October 12, 2021 #D-0092-2022

Product Description

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

Reason for Recall

Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets

Details

Units Affected
a) 124, b) 29, c) 73
Distribution
Nationwide in the US
Location
Burbank, CA

Frequently Asked Questions

What product was recalled?
Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504. Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals. Units affected: a) 124, b) 29, c) 73.
Why was this product recalled?
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Which agency issued this recall?
This recall was issued by the FDA Drug on November 10, 2021. Severity: Critical. Recall number: D-0092-2022.