FDA Device recall Z-0126-2023
EMPOWER 3D Knee Tibial Insert, REF: 341-14-708
- FDA Device
- Class II
- ongoing
- Published 2022-11-02
On 2022-11-02 the FDA classified a Class II recall of EMPOWER 3D Knee Tibial Insert, REF: 341-14-708 by Encore Medical, citing hip liner implant boxes may contain knee inserts and knee insert boxes may contain hip liner implants, which may lead to implants not being available for surgeries, which may caus….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0126-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-08-12 |
| Published | 2022-11-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Encore Medical |
| Distribution | US |
Product
EMPOWER 3D Knee Tibial Insert, REF: 341-14-708. Orthopedic implant component.
Reason
Hip liner implant boxes may contain knee inserts and knee insert boxes may contain hip liner implants, which may lead to implants not being available for surgeries, which may cause delays in surgery.
Identifiers
| code_info | UDI-DI/Lot: 00888912167055/132T1085 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0126-2023%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.