Howmedica recalls rHead Recon Extended Stem Size 3 orthopedic 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 its rHead Recon Extended Stem Size 3 orthopedic implant for replacement of the radius proximal end. The recall is because studies show this implant has a higher revision rate than other similar devices, which could mean it doesn't work as expected after surgery.
This implant has a higher revision rate than other radial head replacements based on medical literature. Revision rate means the implant may need to be replaced again after the initial surgery. This could lead to complications or additional surgery.
Patients who received this implant during surgery are likely affected. Those with the implant are at risk of needing additional surgery if the implant fails.
The product is labeled as 'rHead Recon Extended Stem Size 3' and is part of the Stryker rHead Radial Head and Uni-Elbow system. It was sold with part number 410-0302.
Look for the product name 'rHead Recon Extended Stem Size 3' and part number 410-0302 on your implant.
The recall is because studies show this implant has a higher revision rate than other radial head replacements, which means it may not work as expected after surgery.
Check your implant for the product name and part number. If you have the recalled item, contact Howmedica for further instructions.
The recall indicates a higher revision rate, but the implant itself is not considered dangerous in normal use. Additional surgery may be needed if it fails.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2709-2018 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2709-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
