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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Devices and FDA recall records listed on MedWatcher for Encore Medical, LP.
This page covers the devices and recall records listed below, not the complete product catalogue or recall history. A recall may apply only to specific models, lots, or serial numbers.
Device and manufacturer names are linked using official product, UDI, or FDA records. The source links below show the supporting information.
Official records may use a legal name, brand, division, or shortened name. Similar names do not necessarily refer to the same manufacturer.
Due to packaging discrepancy with incorrect product size mixed up.