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Recall Observatory FDA recall evidence

Device product

rHead Stem Implant Plasma Coated, Size 2. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

Z-2678-2018

October 24, 2017

Class II

Product summary

Firm
Howmedica Osteonics Corp.
Event
Event 79315
Status
Terminated
Classification
Class II
Quantity
285
Official record key
device-enforcement:Z-2678-2018

Official wording

Reason: 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.

Code information: 310-2011

Distribution pattern: Distribution US Nationwide.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.