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
- Recalling Firm
- Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
- 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.
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