D-1719-2015 Class II Terminated

Recalled by The Compounding Pharmacy of America — Knoxville, TN

Recall Details

Product Type
Drugs
Report Date
September 23, 2015
Initiation Date
June 2, 2015
Termination Date
February 10, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
13 ml

Product Description

TRI-MIX (1/1/40) (MFG) Injectable, Multi-Dose Vial, Sterile, Keep Frozen, The Compounding Pharmacy of America, Knoxville, TN

Reason for Recall

Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility

Distribution Pattern

Nationwide

Code Information

All lots distributed between November 2014 and May 2015; 03042015@7, 8/31/2015