FDA Drug recall D-0937-2017
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: 5…
- FDA Drug
- Class II
- terminated
- Published 2017-07-12
On 2017-07-12 the FDA classified a Class II recall of 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: 5… by American Pharmaceutical Ingredients, citing CGMP Deviations: Lack of quality assurance at the API manufacturer.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0937-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-26 |
| Published | 2017-07-12 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | American Pharmaceutical Ingredients |
| Distribution | US |
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
CGMP Deviations: Lack of quality assurance at the API manufacturer.
Identifiers
| code_info | Lots: MCMR1308029NS, MCMR1308029NS-4202015; Exp. 08/18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0937-2017%22
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