Reported Oct 10, 2018 · Terminated

robaxin-750 (methocarbamol tablets, USP), 750 mg, 100-count bottle, Rx Only, Distributed by

Endo Pharmaceuticals, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Endo Pharmaceuticals, Inc. · 1400 Atwater Dr · Malvern, PA · 19355-8701

Is this the product you have?

robaxin-750 (methocarbamol tablets, USP), 750 mg, 100-count bottle, Rx Only, Distributed by

3 of 3 products

Products covered by this recall
#Product as published
1Endo Pharmaceuticals Inc., Malvern, PA 19355
2Manufactured by: Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274
3NDC 52244-449-10.
Lot codes and dates
    • Lot #: 216702P1
    • Exp 09/20
    • 220409P1
    • Exp 01/21
Amount recalled
2,856 bottles

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Labeling: Incorrect Instructions: Dosage information on the immediate container label incorrectly states "Two to four tablets four times daily." rather than the correct dosage of "Two tablets three times daily."

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Feb 4, 2020 · Data as of Sep 19, 6:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.