FDA Device recall Z-0626-2018
G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and…
- FDA Device
- Class II
- terminated
- Published 2018-02-21
On 2018-02-21 the FDA classified a Class II recall of G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and… by Zimmer Biomet, citing the affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0626-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-25 |
| Published | 2018-02-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
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
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
Identifiers
| code_info | Item #110024464 Lot# 478340 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0626-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.