BRP Pharmaceuticals Recalls Methocarbamol 500mg Tablets Due to Strength Label Error
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.
Lower-risk recall
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/35785-brp-pharmaceuticals-recalls-methocarbamol-500mg-tablets-due-to-strength-label.
Source Summary by GovInfoNow · govinfonow.com/recall/35785-brp-pharmaceuticals-recalls-methocarbamol-500mg-tablets-due-to-strength-label · Updated August 18, 2026 · FDA enforcement record: FDA #D-0092-2022
Cite this page
“BRP Pharmaceuticals Recalls Methocarbamol 500mg Tablets Due to Strength Label Error.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35785-brp-pharmaceuticals-recalls-methocarbamol-500mg-tablets-due-to-strength-label. Based on FDA recall #D-0092-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0092-2022%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
BRP Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Verify the NDC number on the bottle to confirm if it matches the recalled numbers: 7133517952, 7133517954, or 7133517957.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the US” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 29 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
Where this comes from
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.
- Official source: FDA Recall #D-0092-2022 (October 12, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0092-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.