Howmedica recalls rHead Recon Stem Implant 6: Higher revision rates than other radial head replacements may lead to implant failure 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.
Howmedica is recalling a specific orthopedic implant for radius joint replacement due to higher-than-expected revision rates after surgery. This means the implant might not work as intended following the procedure, potentially requiring additional surgery.
The implant has been found to have higher revision rates compared to other similar implants. This means it may not function properly after surgery, leading to the need for another procedure to replace it.
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 Stem Implant 6mm Collar, Size 1' and was used in the Stryker rHead Radial Head and Uni-Elbow system. It was sold under the product code 310-2022.
If you had this specific implant during surgery, contact your surgeon to confirm if it's recalled.
The recall states higher revision rates than other implants, but it's not considered immediately dangerous. It may require additional surgery if it fails.
No, the recall does not require stopping use. Patients should follow up with their surgeon if they have concerns.
Look for the product label 'rHead Recon Stem Implant 6mm Collar, Size 1' in the Stryker rHead Radial Head and Uni-Elbow system, with product code 310-2022.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2689-2018 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2689-2018 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.
