Howmedica recalls bipolar stem implants for potential higher revision rates post-surgery. Learn if your Stryker rHead Radial Head implant is affected and what to do.
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.
Howmed: Howmedica Osteonics recalls a specific bipolar stem implant used in radius joint replacements due to higher-than-expected revision rates after surgery. This means the implant may not function as intended following surgery, potentially requiring additional procedures.
The implant has a higher revision rate than other similar devices based on medical literature. Revision means the implant needs to be removed and replaced, which can cause additional surgery and recovery time.
Patients who received the Stryker rHead Radial Head implant system with this specific bipolar stem implant (model RCN-S3) are affected. Those who have undergone radius joint replacement surgery are most at risk.
Check if your implant is labeled 'RCN-S3' and part of the Stryker rHead Radial Head system. This specific bipolar stem implant is used for radius joint replacements.
Look for the model number RCN-S3 on your implant packaging or device.
The recall indicates a higher revision rate than other similar implants, but it does not mean the implant causes injury. Revision means it may need to be replaced after surgery.
No, this is a recall for potential higher revision rates, not an immediate safety hazard. You do not need to stop using it unless your doctor advises otherwise.
Check for the model number RCN-S3 on your implant packaging or device, and confirm it's part of the Stryker rHead Radial Head system.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2718-2018 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2718-2018 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.
