Medications & Supplements/Prescription Drugs

Methocarbamol Tablets Recalled for Incorrect Strength Labeling

Agency Publication Date: November 2, 2021

Summary

Bryant Ranch Prepack is recalling Methocarbamol (methocarbamol) tablets because bottles labeled as 500 mg strength may actually contain 750 mg tablets. The recall affects 124 bottles of 30-count tablets, 29 bottles of 60-count tablets, and 73 bottles of 90-count tablets. No incidents or injuries have been reported to date; however, taking a higher dose than prescribed can lead to increased side effects such as drowsiness and confusion.

Risk

Taking 750 mg of methocarbamol when 500 mg was intended increases the risk of side effects like extreme drowsiness, dizziness, and coordination issues. These effects can significantly impair the ability to drive or operate machinery, potentially leading to accidents.

What You Should Do

This recall affects Methocarbamol 500 mg tablets, labeled with Prinston Laboratories and Bryant Ranch Prepack, which may actually contain higher-strength 750 mg tablets.
Check your bottle to see if it matches the affected lot number 163935 with an expiration date of 10/31/2022.
Identify the National Drug Code (NDC) printed on the bottle: 7133517952 (30-count), 7133517954 (60-count), or 7133517957 (90-count).
If you have health concerns about your medication, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Bryant Ranch Prepack directly for further instructions.
Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

Your Remedy Options

You have 2 options:

Option 1: Full Refund

How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund

Option 2: Dispose of Product

How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Methocarbamol 500mg Tablet

Variants: 30 count, 60 count, 90 count, 750 mg content

Lot Numbers:

163935 (Exp 10/31/2022)

NDC:

7133517952

7133517954

7133517957

Bottles labeled as 500 mg strength actually contain 750 mg tablets.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 88861

Status: Resolved

Manufacturer: Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Sold By: Prinston Laboratories; Bryant Ranch Prepack; BRP Pharmaceuticals

Manufactured In: United States

Units Affected: a) 124, b) 29, c) 73

Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

This recall affects Methocarbamol 500 mg tablets, labeled with Prinston Laboratories and Bryant Ranch Prepack, which may actually contain higher-strength 750 mg tablets.

Check your bottle to see if it matches the affected lot number 163935 with an expiration date of 10/31/2022.

Identify the National Drug Code (NDC) printed on the bottle: 7133517952 (30-count), 7133517954 (60-count), or 7133517957 (90-count).

If you have health concerns about your medication, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Bryant Ranch Prepack directly for further instructions.

Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

Your Remedy Options

You have 2 options:

Option 1: Full Refund

How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund

Option 2: Dispose of Product

How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 88861

Status: Resolved

Manufacturer: Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Sold By: Prinston Laboratories; Bryant Ranch Prepack; BRP Pharmaceuticals

Manufactured In: United States

Units Affected: a) 124, b) 29, c) 73

Distributed To: Nationwide