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Encore Medical Recalls
99 recalls on record · August 15, 2012 to July 15, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 15, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Descr
Hazard: Due to packaging discrepancy with incorrect product size mixed up.
July 15, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Descr
Hazard: Due to packaging discrepancy with incorrect product size mixed up.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/C
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
Hazard: Knee and Humeral socket implants contain incorrect labeling.
March 4, 2026Medical DevicesFDA
Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Mo
Hazard: Knee and Humeral socket implants contain incorrect labeling.
February 11, 2026Medical DevicesFDA
Encore Medical, LP recalls EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H, REF: 942-01-36H; Liner, 10 degree Hooded, HXe+, 36J, REF:
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.
February 11, 2026Medical DevicesFDA
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert 5R 14MM, VE, REF: 342-14-705
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.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE Model/Catalog Number: 804-06-310
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm Model/Catalog Number: 8
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311 Pr
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
August 20, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 34
Hazard: Knee implants contain incorrect labeling (size and/or side incorrect)
August 20, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 34
Hazard: Knee implants contain incorrect labeling (size and/or side incorrect)
July 30, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 Model/Catal
Hazard: Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
July 30, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catal
Hazard: Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
July 23, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 12MM, VE Model/Catalog Numbe
Hazard: 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 revision surgery if used.
July 23, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 10MM, VE Model/Catalog Numbe
Hazard: 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 revision surgery if used.
July 2, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm Model/Catalog Number: 506-04-1
Hazard: Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
July 2, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 18mm Model/Catalog Number: 506-04-1
Hazard: Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
July 2, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm Model/Catalog Number: 506-04-1
Hazard: Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
July 2, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number: 506-04-1
Hazard: Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
January 1, 2025Medical DevicesFDA
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert, 5R 16MM, VE, REF: 342-16-705; EMPOWR 3D Knee Tibial Insert, 3R 14MM, VE, REF: 342-14-703
Hazard: 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.
January 1, 2025Medical DevicesFDA
Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706
Hazard: Knee insert package may contain an acetabular system, which may cause surgical delay to get a new product.
January 10, 2024Medical DevicesFDA
Encore Medical, LP recalls REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2
Hazard: Mislabeling
January 10, 2024Medical DevicesFDA
Encore Medical, LP recalls Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
Hazard: Mislabeling
December 20, 2023Medical DevicesFDA
Encore Medical, LP recalls RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
Hazard: Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
December 13, 2023Medical DevicesFDA
Encore Medical, LP recalls DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated SIZE 8 Left 3D MATRIX COATED REF 243-01-108 DJO
Hazard: Due to incorrect product/device within packaging.
November 15, 2023Medical DevicesFDA
Encore Medical, LP recalls RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component.
Hazard: Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could cause a delay in surgery.
November 15, 2023Medical DevicesFDA
Encore Medical, LP recalls RSP Humeral Small Socket Insert Size 32 mm Semi-Constrained +4, e-plus, REF: 509-03-432, orthopedic shoulder implant com
Hazard: Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could cause a delay in surgery.
November 15, 2023Medical DevicesFDA
Encore Medical, LP recalls DJO EMPOWR Knee Punch Handle, REF: 801-05-040
Hazard: Knee punch handle tip is breaking during surgery due to the lack of heat treatment, which may lead to a disruption in surgery.