Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0626-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: August 25, 2017

Date Posted: February 21, 2018

Recall Number: Z-0626-2018

Event ID: 79104

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.

Status: Terminated

Product Quantity: 8

Code Information:

Item #110024464 Lot# 478340

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated