EMPOWER 3D Knee Tibial Insert, REF: 341-14-708. Orthopedic implant component. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EMPOWER 3D Knee Tibial Insert, REF: 341-14-708. Orthopedic implant component.
Lot Codes / Batch Numbers
UDI-DI/Lot: 00888912167055/132T1085
Products Sold
UDI-DI/Lot: 00888912167055/132T1085
A medical device manufacturer is recalling EMPOWER 3D Knee Tibial Insert, REF: 341-14-708. Orthopedic implant component. due to 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 . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On 8/12/22, recall notices were emailed to DJO Surgical Agents who were informed to do the following: 1) Pass the notice to all those within your organization or to any organization where the potentially affected devices have been transferred. 2) Return affected devices 3) Complete and return the response form Questions, contact: Julie.Baker@Enovis.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026