FDAClass IIAugust 15, 2018

Radial Head Assy recall

Radial Head Assy Size #2, Rad. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow…

Why was Radial Head Assy 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?

410-0004

Product
Radial Head Assy Size #2, Rad. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow…
Recalling firm
Howmedica Osteonics Corp.
Quantity
128
Distribution
Distribution US Nationwide.
Recall date
August 15, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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