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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

Endo Pharmaceuticals, Inc.: Robaxin-750 (methocarbamol) Recalled for Incorrect Dosage Instructions

Agency Publication Date: October 1, 2018
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Summary

Endo Pharmaceuticals, Inc. is recalling 2,856 bottles of Robaxin-750 (methocarbamol tablets, USP), 750 mg, in 100-count bottles. The labels on these bottles incorrectly instruct patients to take "Two to four tablets four times daily" when the correct dosage should be "Two tablets three times daily." This labeling error could lead consumers to take a much higher dose than intended, which may be unsafe.

Risk

Following the incorrect instructions on the label could result in an accidental overdose of methocarbamol. This medication is a muscle relaxant, and taking too much can cause symptoms such as extreme drowsiness, dizziness, or other serious health complications.

What You Should Do

  1. Check your medicine cabinet for 100-count bottles of Robaxin-750 (methocarbamol tablets, USP), 750 mg, with NDC 52244-449-10.
  2. Verify if your bottle belongs to the affected lots: Lot 216702P1 with an expiration date of September 2020 (09/20) or Lot 220409P1 with an expiration date of January 2021 (01/21).
  3. Do not follow the dosage instructions printed on the container label of these specific lots.
  4. Contact your healthcare provider or pharmacist immediately for guidance on the correct dosage for your condition.
  5. Return any unused product to the pharmacy where it was purchased for a refund.
  6. Contact the manufacturer, Endo Pharmaceuticals, Inc., for further instructions.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: Robaxin-750 (methocarbamol tablets, USP), 750 mg, 100-count bottle
Model:
NDC 52244-449-10
Lot Numbers:
216702P1 (Exp 09/20)
220409P1 (Exp 01/21)
Date Ranges: September 2020, January 2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81034
Status: Resolved
Manufacturer: Endo Pharmaceuticals, Inc.
Sold By: Pharmacies
Manufactured In: United States
Units Affected: 2,856 bottles
Distributed To: Nationwide
Agency Last Updated: October 9, 2018

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 ยท 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.