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Recall Observatory FDA recall evidence

Device product

rHead Recon Stem Implant non-coated, Size 4. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

Z-2721-2018

October 24, 2017

Class II

Product summary

Firm
Howmedica Osteonics Corp.
Event
Event 79315
Status
Terminated
Classification
Class II
Quantity
118
Official record key
device-enforcement:Z-2721-2018

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: RCN-S460

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.