Otto Bock Healthcare Product: Medical Device Recall in 2018 - (Recall #: Z-0815-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

OTTO BOCK Kenevo knee joints Model 3C60=ST

Product Classification:

Class II

Date Initiated: September 12, 2017

Date Posted: March 7, 2018

Recall Number: Z-0815-2018

Event ID: 79019

Reason for Recall:

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.

Status: Terminated

Product Quantity: 4

Code Information:

Serial Numbers: 201520028, 201520027, 20150026, and 201530040,

Distribution Pattern:

AK, AR, AZ, CA, CT, DC, GA, IL, IN, KY, LA, MD, MI, MN, NC, ND, NJ, MN, NY, OH, OK, OR, PA, PR, TX, VA, and WA AU, BE, DE, FR, GB, IT, KW, LU, NL, NO, AT, SA, SE, CH, ES, ZA, and HU

Voluntary or Mandated:

Voluntary: Firm initiated