Reviewed V1 category

Knee implants

Implantable components and systems used in knee replacement procedures.

FDA product codes and descriptions are normalized into this consumer-facing category. Raw regulator terminology remains source evidence rather than separate public category pages.

3 tracked devices · 7 recall records

Devices in this category

DePuy Synthes ATTUNE Knee System

DePuy Synthes · Knee implants

Active recall record

Last checked Oct 8, 2026

Stryker Triathlon Knee System

Stryker Corporation · Knee implants

No recall records found

Last checked Aug 17, 2026

Zimmer Biomet Persona Knee System

Zimmer Biomet · Knee implants

No recall records found

Last checked Aug 17, 2026

Recent recall records

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

Class II recallOngoing

DePuy Synthes ATTUNE Knee System recall — FDA event 99078

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

FDA · FDA event 99078Posted Jun 29, 2026DePuy Synthes ATTUNE Knee System

Class II recallOngoing

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

FDA · FDA event 99073Posted Jun 24, 2026

Class II recallOngoing

TRI TS BASEPLATE SIZE 3 recall — FDA event 99080

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as…

FDA · FDA event 99080Posted Jun 17, 2026

Class II recallOngoing

DePuy Synthes ATTUNE Knee System recall — FDA event 98707

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

FDA · FDA event 98707Posted Apr 29, 2026DePuy Synthes ATTUNE Knee System

Class II recallOngoing

Endo-Model SL Connection Component incl recall — FDA event 98342

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

FDA · FDA event 98342Posted Mar 10, 2026

Class II recallOngoing

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.

FDA · FDA event 97971Posted Dec 9, 2025

Manufacturers in this category

Manufacturers are listed because their devices appear in monitored sources. Listing does not imply endorsement or partnership.

Related guides

No guides reference this category yet. Browse all guides.

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Reviewed V1 category

Knee implants

Implantable components and systems used in knee replacement procedures.

FDA product codes and descriptions are normalized into this consumer-facing category. Raw regulator terminology remains source evidence rather than separate public category pages.

3 tracked devices · 7 recall records

Devices in this category

DePuy Synthes ATTUNE Knee System

DePuy Synthes · Knee implants

Active recall record

Last checked Oct 8, 2026

Stryker Triathlon Knee System

Stryker Corporation · Knee implants

No recall records found

Last checked Aug 17, 2026

Zimmer Biomet Persona Knee System

Zimmer Biomet · Knee implants

No recall records found

Last checked Aug 17, 2026

Recent recall records

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

Class II recallOngoing

DePuy Synthes ATTUNE Knee System recall — FDA event 99078

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

FDA · FDA event 99078Posted Jun 29, 2026DePuy Synthes ATTUNE Knee System

Class II recallOngoing

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

FDA · FDA event 99073Posted Jun 24, 2026

Class II recallOngoing

TRI TS BASEPLATE SIZE 3 recall — FDA event 99080

FDA · FDA event 99080Posted Jun 17, 2026

Class II recallOngoing

DePuy Synthes ATTUNE Knee System recall — FDA event 98707

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

FDA · FDA event 98707Posted Apr 29, 2026DePuy Synthes ATTUNE Knee System

Class II recallOngoing

Endo-Model SL Connection Component incl recall — FDA event 98342

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

FDA · FDA event 98342Posted Mar 10, 2026

Class II recallOngoing

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.

FDA · FDA event 97971Posted Dec 9, 2025

Manufacturers in this category

Manufacturers are listed because their devices appear in monitored sources. Listing does not imply endorsement or partnership.

Related guides

No guides reference this category yet. Browse all guides.

Knee implants

Follow Knee implants

Devices in this category

DePuy Synthes ATTUNE Knee System

Stryker Triathlon Knee System

Zimmer Biomet Persona Knee System

Recent recall records

EMPOWR 3D KNEE INS, 11L 14MM, VE recall — FDA event 98700

DePuy Synthes ATTUNE Knee System recall — FDA event 99078

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

TRI TS BASEPLATE SIZE 3 recall — FDA event 99080

DePuy Synthes ATTUNE Knee System recall — FDA event 98707

Endo-Model SL Connection Component incl recall — FDA event 98342

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

Manufacturers in this category

Related guides

Knee implants

Follow Knee implants

Devices in this category

DePuy Synthes ATTUNE Knee System

Stryker Triathlon Knee System

Zimmer Biomet Persona Knee System

Recent recall records

EMPOWR 3D KNEE INS, 11L 14MM, VE recall — FDA event 98700

DePuy Synthes ATTUNE Knee System recall — FDA event 99078

Persona Revision Trabecular Metal Femoral Distal Augment recall — FDA event 99073

TRI TS BASEPLATE SIZE 3 recall — FDA event 99080

DePuy Synthes ATTUNE Knee System recall — FDA event 98707

Endo-Model SL Connection Component incl recall — FDA event 98342

Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, recall — FDA event 97971

Manufacturers in this category

Related guides