PlainRecalls
FDA Drug Moderate Class II Terminated

Omnitrope 17.4U/10mL Inj-Kit, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

Reported: December 9, 2015 Initiated: October 19, 2015 #D-0440-2016

Product Description

Omnitrope 17.4U/10mL Inj-Kit, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

Reason for Recall

Lack of Assurance of Sterility

Details

Recalling Firm
Western Drug
Units Affected
18 containers
Distribution
Nationwide in US: Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah
Location
Springerville, AZ

Frequently Asked Questions

What product was recalled?
Omnitrope 17.4U/10mL Inj-Kit, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938. Recalled by Western Drug. Units affected: 18 containers.
Why was this product recalled?
Lack of Assurance of Sterility
Which agency issued this recall?
This recall was issued by the FDA Drug on December 9, 2015. Severity: Moderate. Recall number: D-0440-2016.