Howmedica recalls rHead Standard Extended Stem implants due to higher revision rates than other radial head replacements. This may lead to complications after surgery.
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.
Howmedica is recalling a specific orthopedic implant used in radius joint replacements because studies show it has a higher revision rate than other similar implants. This means the implant might not work as expected after surgery.
The implant has been found to have a higher revision rate than other radial head replacements. Revision means the implant needs to be removed and replaced, which can cause complications after surgery.
Patients who received this implant during surgery are likely affected. Those with the specific model number 410-0103 are most at risk.
Check if you have the rHead Standard Extended Stem, 6mm Collar, Size 4 implant with model number 410-0103. This is part of the Stryker rHead Radial Head and Uni-Elbow system.
Identify if your implant matches the description: rHead Standard Extended Stem, 6mm Collar, Size 4 with model number 410-0103.
The recall states the implant has a higher revision rate than other similar implants, but it does not indicate immediate danger to users.
The recall does not specify a need to stop using the implant; it focuses on potential revision issues after surgery.
The official notice does not provide specific action steps beyond checking if you have the recalled model.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2706-2018 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2706-2018 from Howmedica. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
