PlainRecalls
FDA Devices Critical Class I Terminated

Comprehensive Reverse Shoulder System Humeral Tray Model 115340

Reported: February 22, 2017 Initiated: December 20, 2016 #Z-1103-2017

Product Description

Comprehensive Reverse Shoulder System Humeral Tray Model 115340

Reason for Recall

Higher than anticipated rate of fracturing due to design. Risk of revision surgery due to fracturing.

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
4388
Distribution
Nationwide. CANADA AUSTRALIA CHILE COLOMBIA KOREA Netherlands
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Comprehensive Reverse Shoulder System Humeral Tray Model 115340. Recalled by Zimmer Biomet, Inc.. Units affected: 4388.
Why was this product recalled?
Higher than anticipated rate of fracturing due to design. Risk of revision surgery due to fracturing.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 22, 2017. Severity: Critical. Recall number: Z-1103-2017.