Methocarbamol 500mg Tablet — Class I drug recall D-0092-2022
Completed recall by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals, reported 2021-11-10, distributed nationwide. Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain M
| Recall number | D-0092-2022 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals, Burbank, CA, United States |
| Recall initiated | 2021-10-12 |
| Classified | 2021-11-02 |
| Reported by FDA | 2021-11-10 |
| Distributed | Nationwide (US) |
| Reason classes | labeling, potency |
| Lot numbers | 163935 |
| Expiration dates | 2022-10-31 |
Product
Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504
Reason for recall
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0092-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.