Howmedica recalls rHead Recon Stem Implant Size 3 due to higher revision rates than other radial head replacements. This implant may not perform as expected post-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.
Howmed: The rHead Recon Stem Implant (Size 3) is recalled because studies show it has a higher revision rate than other implants for replacing the radius bone. This means the implant might not work as intended after surgery, potentially requiring additional procedures.
This implant has a higher revision rate than other options for replacing the radius bone. Revision rate refers to how often the implant needs to be replaced after surgery. The implant may not perform as expected, leading to additional surgeries.
Patients who received this specific implant during surgery are likely affected. Those with the implant may need to monitor for complications but are not at immediate risk.
Check if you received the rHead Recon Stem Implant Plasma Coated, Size 3. This implant is part of the Stryker rHead Radial Head and Uni-Elbow system. The recall number is 310-2020.
Reach out to your surgeon to discuss whether you have the recalled implant and next steps.
The recall indicates a higher revision rate than other implants, but it is not immediately dangerous. Patients may need additional surgery if the implant fails.
No immediate action is required. Patients should contact their surgeon to discuss if they have the recalled implant.
Check if you received the rHead Recon Stem Implant Plasma Coated, Size 3 as part of the Stryker rHead Radial Head and Uni-Elbow system. The recall number is 310-2020.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2687-2018 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2687-2018 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.
