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.
Reported: February 21, 2018 Initiated: August 25, 2017 #Z-0626-2018
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.
Details
- Recalling Firm
- Zimmer Biomet, Inc.
- Units Affected
- 8
- Distribution
- US Nationwide Distribution
- Location
- Warsaw, IN
Frequently Asked Questions
What product 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.. Recalled by Zimmer Biomet, Inc.. Units affected: 8.
Why was this product recalled? ▼
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 21, 2018. Severity: Moderate. Recall number: Z-0626-2018.
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