FDAJanuary 5, 2026device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

encore medical lpencoreencore medical

UPCs

00888912167529

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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