PlainRecalls
FDA Drug Moderate Class II Terminated

Baclofen 500 mcg/mL Injectable, 22 mL vial, Compounded by The Compounding Shop, St. Petersburg, FL

Reported: June 12, 2013 Initiated: May 2, 2013 #D-550-2013

Product Description

Baclofen 500 mcg/mL Injectable, 22 mL vial, Compounded by The Compounding Shop, St. Petersburg, FL

Reason for Recall

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Details

Units Affected
1 vial of 22mL
Distribution
Florida, California, Minnesota, and Maine
Location
St Petersburg, FL

Frequently Asked Questions

What product was recalled?
Baclofen 500 mcg/mL Injectable, 22 mL vial, Compounded by The Compounding Shop, St. Petersburg, FL. Recalled by THE COMPOUNDING SHOP, INC.. Units affected: 1 vial of 22mL.
Why was this product recalled?
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 12, 2013. Severity: Moderate. Recall number: D-550-2013.