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Zimmer Biomet, Inc. recalls G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal o
Recalled February 21, 2018 · FDA recall Z-0626-2018 · Zimmer Biomet
Hazard
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners. · FDA Class II
Units
8
Sold at
US Nationwide Distribution
Description
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
Product
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.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →