Class II recallOngoing
EMPOWR 3D KNEE INS, 11L 14MM, VE recall — FDA event 98700
Due to packaging discrepancy with incorrect product size mixed up.
FDA · FDA event 98700Posted Jul 8, 2026
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The FDA identifies Encore Medical, LP as the recalling firm in one or more MedWatcher-reviewed medical-device recall records.
This page includes only canonical device families and FDA recall events separately reviewed for publication by MedWatcher. It is not a complete product catalogue.
Canonical identity is based on the linked official product, UDI, or FDA recalling-firm source. Source-name variants are retained as aliases rather than separate manufacturer pages.
Source databases can use a legal name, brand, division, or shortened name. MedWatcher retains the form used as evidence rather than treating every similar name as the same manufacturer.
Page reviewed Aug 17, 2026 by MedWatcher project owner — FUS-265 · Next review by Nov 15, 2026.
Due to packaging discrepancy with incorrect product size mixed up.