D-0434-2016 Class II Terminated

Recalled by Western Drug — Springerville, AZ

FDA drug recall D-0434-2016 was initiated by Western Drug on October 19, 2015 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated October 1, 2016). Affected quantity: 4 containers.

Recall Details

Product Type
Drugs
Report Date
December 9, 2015
Initiation Date
October 19, 2015
Termination Date
October 1, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4 containers

Product Description

Lidocaine Injection 1% , 2%, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

Reason for Recall

Lack of Assurance of Sterility

Distribution Pattern

Nationwide in US: Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah

Code Information

all lots