OTTO BOCK Kenevo knee joints Model 3C60 — Class II medical device recall Z-0814-2018
Terminated recall by Otto Bock Healthcare Product, reported 2018-03-07, distributed in AK, AR, AZ, CA, CT, DC, GA, IL…. Otto Bock Healthcare Products GmbH has identified a design issue through extended durability testing where the
| Recall number | Z-0814-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Otto Bock Healthcare Product, Vienna, N/A, Austria |
| Recall initiated | 2017-09-12 |
| Classified | 2018-03-01 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2021-01-19 |
| Distributed | AK, AR, AZ, CA, CT, DC, GA, IL, IN, KY, LA, MD, MI, MN, NC, ND, NJ, NY, OH, OK, OR, PA, PR, TX, VA, WA |
| Quantity | 75 units |
| Reason classes | labeling |
| Serial numbers | 201520002, 201520006, 201520007, 201520008, 201520009, 201520010, 201520011, 201520012, 201520013, 201520027, 201520028, 201522040, 201522043, 201522045, 201522046, 201524050, 201524051, 201525069, 201525109, 201528134, 201528139, 201549087, 201550012, 201550014, 201550016 and 57 more |
| Model numbers | 3C60 |
Product
OTTO BOCK Kenevo knee joints Model 3C60
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0814-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.