Methocarbamol — Class II drug recall D-0937-2017
Terminated recall by American Pharmaceutical Ingredients LLC, reported 2017-07-12, distributed nationwide. CGMP Deviations: Lack of quality assurance at the API manufacturer.
| Recall number | D-0937-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Pharmaceutical Ingredients LLC, Waterford, MI, United States |
| Recall initiated | 2017-05-26 |
| Classified | 2017-07-02 |
| Reported by FDA | 2017-07-12 |
| Terminated | 2018-05-31 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| NDC | 58597-8023-06, 58597-8023-07, 58597-8023-08 |
| Lot numbers | 08/18, MCMR1308029NS, MCMR1308029NS-4202015 |
Product
Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327
Reason for recall
CGMP Deviations: Lack of quality assurance at the API manufacturer.
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-0937-2017. 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.