Z-0626-2018 Class II Terminated

Recalled by Zimmer Biomet, Inc. — Warsaw, IN

Recall Details

Product Type
Devices
Report Date
February 21, 2018
Initiation Date
August 25, 2017
Termination Date
August 16, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
8

Product Description

G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal function and mobility to the damaged joint.

Reason for Recall

The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.

Distribution Pattern

US Nationwide Distribution

Code Information

Item #110024464 Lot# 478340