Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0814-2018 — OTTO BOCK Kenevo knee joints Model 3C60

U.S. FDA — Device Enforcement · Austria · 2017-09-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0814-2018
Date of alert
2017-09-12
Country / jurisdiction
Austria
Risk level
Class II
Risk type
recall
Brand
Otto Bock Healthcare Product
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
201520007
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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