Z-2366-2018 Class II Terminated

Recalled by Zimmer Biomet, Inc. — Warsaw, IN

Recall Details

Product Type
Devices
Report Date
July 11, 2018
Initiation Date
May 30, 2018
Termination Date
May 28, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
132

Product Description

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 11; 00-7713-011-00

Reason for Recall

M/L Taper Hip Prosthesis and M/L Taper Hip Prosthesis with Kinectiv Technology manufactured prior to October 2015 are being recalled due to the potential for black residue to be observed within the polyethylene bag containing the implant. The black residue is a combination of the titanium plasma spray used to create the porous surface of the implant and polyethylene bag containing the implant. The recalling firm states the residue is biocompatible. Risks include delay of surgery while locating a replacement device, and surgical intervention due to wear caused by debris.

Distribution Pattern

Products were distributed solely to Japan.

Code Information

62432961 62848695 62914651 62927105 62927112 63068929 63081264 63090024 63090028 63116798 63161432