Zimmer Biomet, Inc. Recall: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use
Zimmer Biomet, Inc. Recall: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Zimmer Biomet, Inc.; Product: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of
| Recalling firm | Zimmer Biomet, Inc. |
|---|---|
| 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. |
| 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. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide Distribution |
| Recall initiated | 20170825 |
| Recall number | Z-0626-2018 |
| Category | device |
| State | IN |
| Country | United States |
$29/mo
Try RecallGuard →