WhichRecall
Class IIReported 2026-02-11

EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705

Recalled by Encore Medical, LP

Reason for Recall

942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay to exchange devices or revision surgery.

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Recall Number
Z-1233-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-01-05
Reported
2026-02-11
Distribution
US: TX, IA, MI, MS, MA, RI, NJ, PA, NY, MO, OK, PR, AL, CA
Code Info
UDI-DI: 00888912167529. Lot: 139T1075A. Expiration: 03-12-2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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