Home / Brands / Stanmore Implants Worldwide
Stanmore Implants Worldwide Recalls
8 recalls on record · May 18, 2016 to September 13, 2017 · Medical Devices
Recalls by year
16
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 13, 2017Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or de
Hazard: Three (3) complaints were identified in which the potential for utilization of the JTS Grower Drive in the incorrect orientation in relation to the limb entry point of the device, together with the potential to select incorrect settings for the extension procedure. As a result, the prostheses in such cases failed to extend as intended.
December 28, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls DF Coated Integral Shaft & Stem 15x30x38; DF Coated Integral Shaft & Stem 15x36x44; DF Coated Integral Shaft & Ste
Hazard: The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.
December 28, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls Femoral Integral Shaft & Stem 15x27 HA Coated; Femoral Integral Shaft & Stem 15x30 HA Coated; Femoral Integral Shaft
Hazard: The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.
December 28, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls Femoral Shaft L=120mm; Femoral Shaft L=135mm; Femoral Shaft L=150mm The product is a component is a systems that is int
Hazard: The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.
December 28, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls Tibial Component Metal Cased Small Long; Tibial Component Metal Cased Small Short; Tibial Component Metal Cased Std Long
Hazard: The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.
December 28, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a component is a syste
Hazard: The recalling firm has received 5 customer inquiries reporting that at least one pouch of the double pouch packaging configuration has been punctured by the tip of the device's stem.
August 24, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls METS SMILES Total Knee Replacement
Hazard: The manufacturer has identified that the stated Femoral Plateau Plates may not fit into the intended Femoral Knee mating component and thus sit flush upon the Femoral Knee component prior to implantation.
May 18, 2016Medical DevicesFDA
Stanmore Implants Worldwide Ltd. recalls Distal Femoral Replacement (patient specific, custom made orthopedic implant device). PIN 19960
Hazard: Incorrect component used to manufacture distal femoral replacement.