PlainRecalls
FDA Devices Moderate Class II Terminated

Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427 4006(17)220731(10)63694912)

Reported: April 4, 2018 Initiated: January 24, 2018 #Z-1239-2018

Product Description

Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427 4006(17)220731(10)63694912)

Reason for Recall

One lot of humeral stem implants do not include the humeral bushing components.

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
9
Distribution
Distributed in China and Taiwan.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427 4006(17)220731(10)63694912). Recalled by Zimmer Biomet, Inc.. Units affected: 9.
Why was this product recalled?
One lot of humeral stem implants do not include the humeral bushing components.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 4, 2018. Severity: Moderate. Recall number: Z-1239-2018.