Device recall
Z-1733-2022: GXL acetabular liners, orthopedic hip implant component. Product Line Numbers…
FDA device recall · Class II · Exactech, Inc.
Key facts
| Recall number (Z-number) | Z-1733-2022 |
|---|---|
| Recall event | 90279 |
| Product | GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 42, REF 106-22-42; b. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 44, REF 106-22-44; c. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 46, REF 106-22-46; d… |
| Product code | JDI |
| Recalling firm | Exactech, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K963313 |
| FEI number | 1038671 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database