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Integra LifeSciences Recalls
246 recalls on record · June 20, 2012 to March 12, 2025 · 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.
Also filed under
The recall feeds record what looks like the same company under more than one name:
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Left, Product No. LJV193T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Left, Product No. LJV192T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Left, Product No. LJV190T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Right, Product No. LJV183T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Right, Product No. LJV181T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Right, Product No. LJV180T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis, Flat Cut, Size 3, Right, Product No. LJU813T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Right, Product No. LJU812T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Flat Cut, Size 1, Right, Product No. LJU811T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Flat Cut, Size 3, Left, Product No. LJU823T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Left, Product No. LJU822T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Talar Dome Total Ankle Prosthesis, Flat Cut, Size 1, Left, Product No. LJU821T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Tibial Total Ankle Prosthesis Tray, Size 2, Product No. LJU222T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Tibial Total Ankle Prosthesis Tray, Size 1, Product No. LJU221T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Tibial Total Ankle Prosthesis Tray, Size 0, Product No. LJU220T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Left, Part No. LJU213T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Left, Part No. LJU212T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 1, Left, Part No. LJU211T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Left, Part No. LJU210T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Right, Part No. LJU203T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Right, Part No. LJU202T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris Tibial Ankle Prosthesis Tray, Talar Dome, Size 1, Right, Part No. LJU201T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
April 24, 2019Medical DevicesFDA
Integra LifeSciences Corp. recalls Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T
Hazard: The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU
August 8, 2018Medical DevicesFDA
Integra LifeSciences Corp. recalls MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT, Part Number A2600R The MAYFIELD¿ Infinity XR2 Base Unit is intended to be
Hazard: There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
August 8, 2018Medical DevicesFDA
Integra LifeSciences Corp. recalls MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to
Hazard: There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
August 8, 2018Medical DevicesFDA
Integra LifeSciences Corp. recalls MAYFIELD Infinity XR2 Base Unit-Extended, Part Number A2079E The MAYFIELD¿ Infinity XR2 Base Unit is intended to be
Hazard: There is a potential for the knob assembly in the swivel adapter to fracture/break during use.
August 8, 2018Medical DevicesFDA
Integra LifeSciences Corp. recalls MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to su
Hazard: There is a potential for the knob assembly in the swivel adapter to fracture/break during use.