Recall StatusTerminated
Date Initiated2017-09-12
Date Terminated2021-01-19
Product Quantity4
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.
Firm Action
On September 14, 2017 a letter was sent to all their consignees via 2nd day signature receipt required to customers instructing them to contact their patients and send in their devices for service within the first 2.3 years of use. The pylon clamp will be replaced at no charge. The pylon will also be inspected and replaced if necessary. The customer will be requested to complete a reply form indicating they have received the notice and intend to contact their patients to arrange for the requested service.
Customer Service: (800) 328-3458 Option 1
Loaner Service: (800) 328-3458 Option 3, then Option 1
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
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.