RecallRadar

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…

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

AgencyFDA Drug
Recall numberD-0937-2017
ClassificationClass II
Statusterminated
Initiated2017-05-26
Published2017-07-12
Last updated2026-09-13 11:51 UTC
CompanyAmerican Pharmaceutical Ingredients
DistributionUS

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_infoLots: 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

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.