Howmedica recalls rHead Recon Stem Implant Size 2 due to higher revision rates than other radial head replacements. This implant may not perform as expected 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 Stem Implant Size 2 for potential higher revision rates compared to other radial head replacements. This means the implant might not work as intended after surgery.
The implant has been found to have higher revision rates than other similar implants based on medical literature. This means it may not function properly after surgery, requiring additional procedures.
Patients who received this specific implant during surgery are likely affected. Those with the implant are at risk of needing additional surgery if the implant fails.
Check if you received the rHead Recon Stem Implant Plasma Coated, Size 2 as part of the Stryker rHead Radial Head and Uni-Elbow system. The product was sold starting in 2 as indicated by the model number 310-2019.
Review your surgical records to confirm if you received the rHead Recon Stem Implant Plasma Coated, Size 2.
The recall indicates higher revision rates compared to other implants, but it does not mean the implant is dangerous in normal use.
No, the recall does not require stopping use. The implant may still function as intended for most patients.
Check your surgical records for the rHead Recon Stem Implant Plasma Coated, Size 2 as part of the Stryker rHead Radial Head and Uni-Elbow system.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2686-2018 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2686-2018 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.
