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Class I: serious health riskCompleted

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals Methocarbamol 500mg Tablet Recall

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (ND…

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals · Burbank, CA

Risk level
Class I
Reported by FDA
Nov 10, 2021
Recall ID
D-0092-2022
Check your lot numberHow we source this data

Summary

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals recalled Methocarbamol 500mg Tablet starting Oct 12, 2021. The FDA classified it as Class I (serious health risk) and published enforcement report D-0092-2022 on Nov 10, 2021. Reason: Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets. Status: Completed.

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

Lot #: 163935, Exp: 10/31/2022

Where it was sold

Nationwide in the US

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0092-2022
Classification
Class I
Status
Completed
Recall initiated
Oct 12, 2021
FDA report date
Nov 10, 2021
Quantity
a) 124, b) 29, c) 73
Recall type
Voluntary: Firm initiated
Recalling firm
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Original FDA data

Every field from FDA enforcement report D-0092-2022, exactly as published.

Show all FDA fields
City
Burbank
State
CA
Status
Completed
Country
United States
Event ID
88861
Address
1919 N Victory Pl
Code information
Lot #: 163935, Exp: 10/31/2022
Postal code
91504-3425
Report date
Nov 10, 2021
Product type
Drugs
Recall number
D-0092-2022
Classification
Class I
Recalling firm
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Product quantity
a) 124, b) 29, c) 73
Reason for recall
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
Nationwide in the US
Recall initiation date
Oct 12, 2021
Initial firm notification
Letter
Center classification date
Nov 2, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0092-2022, published Nov 10, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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