Encore Medical recalls

Encore Medical has 99 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 15 Jul 2026. 59 are still ongoing. 7 were reported in the last 12 months.

Total recalls99since 2012
Last 12 months7reported
Class I00% of total
Ongoing59latest 15 Jul 2026

Recalls per month, last 24 months

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Severity split

Class I 0 0%Class II 99 100%Class III 0 0%

By year

Ongoing encore medical recalls

59 active

All encore medical recalls, newest first

99 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEmpowr 3d Knee Ins, Ve recalled by Encore MedicalEncore MedicalPackaging Defects14 states
DeviceCLASS IIEmpowr 3d Knee Ins, Ve recalled by Encore MedicalEncore MedicalPackaging Defects14 states
DeviceCLASS IIEmpowr 3d Knee Ins, Ve recalled by Encore MedicalEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIReverse Shoulder Prosthesis recalled by Encore MedicalEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIReverse Shoulder Prosthesis recalled by Encore MedicalEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIEmpowr Acetabular System: Liner, 10 degree Hooded, HXe+, 36H recalledEncore MedicalPackaging Defects14 states
DeviceCLASS IIEmpowr 3D Knee Tibial Insert 5R, VE recalled by Encore MedicalEncore MedicalPackaging Defects14 states
DeviceCLASS IIDjo Surgical Altivate Reverse Wedge Glenoid Reamer Sleeve recalledEncore MedicalOtherNationwide
DeviceCLASS IIDjo Surgical Altivate Reverse Wedge Glenoid Reamer Head recalledEncore MedicalOtherNationwide
DeviceCLASS IIDJO Surgical FA S Altivate Reverse Glenoid Tray recalledEncore MedicalForeign MaterialNationwide
DeviceCLASS IIDjo Surgical Altivate Reverse Wedge Glenoid Reamer Boss Drill recalledEncore MedicalOtherNationwide
DeviceCLASS IIEmpowr 3d Knee Tibial Insert - E-plus Empowr 3d Knee Ins, 7r, Ve recalledEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIEmpowr 3d Knee Tibial Insert - E-plus Empowr 3d Knee Ins, Ve recalledEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIEmpowr Dual Mobility" Empowr Acetabular, Dual Mobility recalledEncore MedicalPackaging Defects17 states
DeviceCLASS IIEmpowr Dual Mobility" Empowr Acetabular, Dual Mobility recalledEncore MedicalPackaging Defects17 states
DeviceCLASS IIEmpowr 3d Knee Tibial Insert - E-plus Empowr 3d Kneetm Ins, Ve recalledEncore MedicalPackaging Defects18 states
DeviceCLASS IIEmpowr 3d Knee Tibial Insert - E-plus Empowr 3d Kneetm Ins, Ve recalledEncore MedicalPackaging Defects18 states
DeviceCLASS IIAltivate Reverse Torx Peripheral Screw recalled by Encore MedicalEncore MedicalPackaging Defects19 states
DeviceCLASS IIAltivate Reverse Torx Peripheral Screw recalled by Encore MedicalEncore MedicalPackaging Defects19 states
DeviceCLASS IIAltivate Reverse Torx Peripheral Screw recalled by Encore MedicalEncore MedicalPackaging Defects19 states
DeviceCLASS IIAltivate Reverse Torx Peripheral Screw recalled by Encore MedicalEncore MedicalPackaging Defects19 states
DeviceCLASS IIEmpowr 3D Knee Tibial Insert, 6R, VE recalled by Encore MedicalEncore MedicalPackaging DefectsNationwide
DeviceCLASS IIEmpowr 3D Knee Tibial Insert, 5R, VE recalled by Encore MedicalEncore MedicalPackaging DefectsNationwide
DeviceCLASS IIREF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, Sterile recalledEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIReverse Shoulder System e+ recalled by Encore MedicalEncore MedicalLabeling ErrorsNationwide
DeviceCLASS IIRSP Glenoid Baseplate P2 Porous Coated recalled by Encore MedicalEncore MedicalOther18 states
DeviceCLASS IIDjo surgical Empowr Porous Knee System Empowr 3D recalledEncore MedicalPackaging DefectsNationwide
DeviceCLASS IIRSP Humeral Small Socket Insert Size Semi-Constrained +4, e-plus recalledEncore MedicalPackaging Defects13 states
DeviceCLASS IIRSP Humeral Socket Insert Size Semi-Constrained + recalledEncore MedicalPackaging Defects13 states
DeviceCLASS IIDJO Empowr Knee Punch Handle recalled by Encore MedicalEncore MedicalDevice Malfunction24 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.