BRP Pharmaceuticals recalls methocarbamol tablets labeled as 500mg but containing 750mg due to labeling error. Consumers should check product details and contact the company for guidance.
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
BRP Pharmaceuticals has recalled methocarbamol tablets that are labeled as 500mg but actually contain 750mg. This labeling error could lead to incorrect dosing and potential health risks if taken without knowing the actual strength.
The tablets are labeled as 500mg but contain 750mg, which could result in an overdose if taken as directed. This labeling error may cause incorrect dosing and health risks, especially for those using the medication for conditions like muscle spasms or seizures.
People who have purchased the recalled methocarbamol tablets from pharmacies or retailers. Those using the medication for muscle spasms or seizures are most at risk due to potential incorrect dosing.
Check for bottles labeled as Methocarbamol 500mg Tablets with NDC numbers 7133517952 (30 count), 7133517954 (60 count), or 7133517957 (90 count). The product is prescription-only and was packaged by Bryant Ranch Prepack in Burbank, CA.
Verify the NDC number on the bottle to confirm if it matches the recalled numbers: 7133517952, 7133517954, or 7133517957.
The product was recalled due to a labeling error where bottles labeled as Methocarbamol 500mg tablets actually contain Methocarbamol 750mg tablets.
Check the NDC number on the bottle to see if it matches the recalled numbers (7133517952, 7133517954, or 7133517957). Contact BRP Pharmaceuticals for further guidance.
The recall is due to a labeling error that could lead to incorrect dosing, but the official notice does not specify a risk of serious injury.
We’ve drafted a message you can send BRP Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0092-2022 — BRP Pharmaceuticals BRP Pharmaceuticals Hello, I own a BRP Pharmaceuticals that is covered by recall D-0092-2022 from BRP Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
