Methocarbamol 500mg Tablet recall: Labeling Error
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
Why was Methocarbamol 500mg Tablet recalled?
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 163935, Exp: 10/31/2022
- Product
- 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
- Recalling firm
- Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
- Quantity
- a) 124, b) 29, c) 73
- Distribution
- Nationwide in the US
- Recall date
- November 10, 2021
- Classification
- Class I
- Status
- Completed
- Agency
- FDA (drug)