PlainRecalls
FDA Drug Moderate Class II Terminated

Rescue solution with triamcinolone (lidocaine, bupivacaine, heparin, triamcinolone) injection solution packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.

Reported: November 5, 2014 Initiated: August 27, 2014 #D-0131-2015

Product Description

Rescue solution with triamcinolone (lidocaine, bupivacaine, heparin, triamcinolone) injection solution packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.

Reason for Recall

Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.

Details

Units Affected
27 mL
Distribution
Nationwide
Location
Naperville, IL

Frequently Asked Questions

What product was recalled?
Rescue solution with triamcinolone (lidocaine, bupivacaine, heparin, triamcinolone) injection solution packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.. Recalled by Martin Avenue Pharmacy, Inc.. Units affected: 27 mL.
Why was this product recalled?
Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 5, 2014. Severity: Moderate. Recall number: D-0131-2015.