Medical DeviceJul 15, 2026
EMPOWR 3D KNEE INS, 11L 14MM, VE recall — FDA Z-2700-2026
Due to packaging discrepancy with incorrect product size mixed up.
Class IIFDA: OngoingEncore Medical, LP
Recall history in this database
Classification mix: Class II: 5.
Medical DeviceJul 15, 2026
EMPOWR 3D KNEE INS, 11L 14MM, VE recall — FDA Z-2701-2026
Due to packaging discrepancy with incorrect product size mixed up.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 4, 2026
Reverse Shoulder Prosthesis (RSP) RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus recall — FDA Z-1458-2026
Knee and Humeral socket implants contain incorrect labeling.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 4, 2026
Reverse Shoulder Prosthesis (RSP) RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus recall — FDA Z-1460-2026
Knee and Humeral socket implants contain incorrect labeling.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 4, 2026
EMPOWR 3D KNEE INS, 7L 16MM, VE recall — FDA Z-1459-2026
Knee and Humeral socket implants contain incorrect labeling.
Class IIFDA: OngoingEncore Medical, LP
Understanding this recall history
This page summarizes recall records in which the official source identifies Encore Medical, LP as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.