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Otto Bock Healthcare Product Recalls

3 recalls on record · September 2, 2015 to March 7, 2018 · Medical Devices

Recalls by year

15
18

Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

March 7, 2018Medical DevicesFDA
Otto Bock Healthcare Product recalls OTTO BOCK Kenevo knee joints Model 3C60=ST
Hazard: Otto Bock Healthcare Products GmbH has identified a design issue through extended durability testing where the pylon clamping mechanism has the potential to cause damage to the pylon. When used longer than 1.45 million cycles (which represents approximately 2.3 years of use of the knee joint under heavy usage conditions), AND the pylon clamp is overtightened according to the labeled torque specification, AND the patient weighs at most 125kg it may be remote that the pylon breaks, and causing the patient to fall. There have been no failures or complaints reported directly attributed to the failure mode collapsed pylon. In the US Market and in Canada, labeling requires a condition based service at three years. In the rest of the world, a mandatory two year service interval is specified. Only the devices in distribution in the United States and Canada are affected by this action.
March 7, 2018Medical DevicesFDA
Otto Bock Healthcare Product recalls OTTO BOCK Kenevo knee joints Model 3C60
Hazard: Otto Bock Healthcare Products GmbH has identified a design issue through extended durability testing where the pylon clamping mechanism has the potential to cause damage to the pylon. When used longer than 1.45 million cycles (which represents approximately 2.3 years of use of the knee joint under heavy usage conditions), AND the pylon clamp is overtightened according to the labeled torque specification, AND the patient weighs at most 125kg it may be remote that the pylon breaks, and causing the patient to fall. There have been no failures or complaints reported directly attributed to the failure mode collapsed pylon. In the US Market and in Canada, labeling requires a condition based service at three years. In the rest of the world, a mandatory two year service interval is specified. Only the devices in distribution in the United States and Canada are affected by this action.
September 2, 2015Medical DevicesFDA
Otto Bock Healthcare Product recalls Otto Bock Healthcare Products GmbH Genium X3 Model Number: 3B5-2, Manufacturer Otto Bock Healthcare Products GmbH.
Hazard: Otto Bock Healthcare Products GmbH is recalling the new Genium X3 knee joint prosthesis due to issues with the resistance-control of the hydraulics, which may fail under conditions.
Otto Bock Healthcare Product Recalls | RecallWatchUSA