FDAClass IIAugust 15, 2018

rHead Stem Implant Plasma Coated recall

rHead Stem Implant Plasma Coated, Size 4. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and…

Why was rHead Stem Implant Plasma Coated recalled?

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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

310-2013

Product
rHead Stem Implant Plasma Coated, Size 4. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and…
Recalling firm
Howmedica Osteonics Corp.
Quantity
301
Distribution
Distribution US Nationwide.
Recall date
August 15, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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