PlainRecalls
FDA Devices Moderate Class II Terminated

Amplatz Ultra Stiff Wire Guide

Reported: March 21, 2018 Initiated: October 13, 2017 #Z-0950-2018

Product Description

Amplatz Ultra Stiff Wire Guide

Reason for Recall

Label does not state that the product is heparin-coated.

Details

Recalling Firm
Cook Inc.
Units Affected
12,462
Distribution
Nationally
Location
Bloomington, IN

Frequently Asked Questions

What product was recalled?
Amplatz Ultra Stiff Wire Guide. Recalled by Cook Inc.. Units affected: 12,462.
Why was this product recalled?
Label does not state that the product is heparin-coated.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 21, 2018. Severity: Moderate. Recall number: Z-0950-2018.