Zimmer Biomet, Inc. recalls G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of t…

Recall date

August 25, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0626-2018

FDA classification

Class II

Brand / firm

Zimmer Biomet, Inc.

Sold / distributed

US Nationwide Distribution

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.