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: 64.
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
Medical DeviceFeb 11, 2026
Encore Medical EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705 recall — FDA Z-1233-2026
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,…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceFeb 11, 2026
Encore Medical EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H, REF: 942-01-36H recall — FDA Z-1234-2026
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,…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceSep 17, 2025
DJO SURGICAL ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm recall — FDA Z-2547-2025
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceSep 17, 2025
DJO SURGICAL FA S Altivate Reverse Glenoid Tray recall — FDA Z-2549-2025
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceSep 17, 2025
DJO SURGICAL ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD recall — FDA Z-2546-2025
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceSep 17, 2025
DJO SURGICAL ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE recall — FDA Z-2548-2025
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceAug 20, 2025
EMPOWR 3D KNEE INS, 4L 16MM, VE recall — FDA Z-2285-2025
Knee implants contain incorrect labeling (size and/or side incorrect)
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceAug 20, 2025
EMPOWR 3D KNEE INS, 7R 16MM, VE recall — FDA Z-2286-2025
Knee implants contain incorrect labeling (size and/or side incorrect)
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 30, 2025
EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 recall — FDA Z-2147-2025
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 30, 2025
EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 recall — FDA Z-2148-2025
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 23, 2025
EMPOWR 3D KNEETM INS, 11L 12MM, VE recall — FDA Z-2126-2025
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. The use of this product may result in the incorrect product being selected. This could result in a…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 23, 2025
EMPOWR 3D KNEETM INS, 11L 10MM, VE recall — FDA Z-2125-2025
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. The use of this product may result in the incorrect product being selected. This could result in a…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 2, 2025
ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm recall — FDA Z-2008-2025
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 2, 2025
ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm recall — FDA Z-2011-2025
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 2, 2025
ALTIVATE REVERSE TORX PERIPHERAL SCREW, 18mm recall — FDA Z-2010-2025
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJul 2, 2025
ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm recall — FDA Z-2009-2025
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJan 1, 2025
Encore Medical EMPOWR 3D Knee Tibial Insert, 5R 16MM, VE, REF: 342-16-705 recall — FDA Z-0766-2025
5R 16MM knee tibial insert package may contain knee tibial insert 3R 14MM and vice versa, which may cause surgical delay to get a new product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceJan 1, 2025
Encore Medical EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706 recall — FDA Z-0761-2025
Knee insert package may contain an acetabular system, which may cause surgical delay to get a new product.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceDec 20, 2023
Encore Medical RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204 recall — FDA Z-0532-2024
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
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.