FDA recall Z-2732-2018

Howmedica Osteonics Corp. · Class II · device

Product

rHead, Radial Implant 6 mm Collar, Size 4. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

Reason for recall

Revision rate identified as higher than other proximal radial head replacement devices based on literature review. Product may not perform at expected level post-surgery.

Distribution

Distribution US Nationwide.

Key facts

Status
Terminated
Initiation date
2017-10-24
Report date
2018-08-15
Termination date
2023-05-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mahwah, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2732-2018