PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: July 12, 2017 Initiated: May 26, 2017 #D-0937-2017

Product Description

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.

Details

Units Affected
5,000g (5 kg)
Distribution
Nationwide
Location
Waterford, MI

Frequently Asked Questions

What product was recalled?
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. Recalled by American Pharmaceutical Ingredients LLC. Units affected: 5,000g (5 kg).
Why was this product recalled?
CGMP Deviations: Lack of quality assurance at the API manufacturer.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 12, 2017. Severity: Moderate. Recall number: D-0937-2017.