Encore Medical recalls ALTIVATE REVERSE Torx Peripheral screws (model 506-04-118) due to incorrect size labeling on packaging. This may lead to improper use in shoulder replacements.
Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.
Encore Medical is recalling their ALTIVATE REVERSE Tor: 18mm Torx peripheral screws (model 506-04-118) because the packaging labels show a different size than the actual product. This could cause improper use in shoulder replacements, potentially leading to complications.
The packaging labels for these screws indicate a different size than the actual product. This mismatch could lead to improper installation during surgery, potentially causing complications in shoulder replacements.
Patients who have received shoulder replacements using these screws are affected. Surgeons and medical staff who use these screws during procedures are at risk.
Check for the model number 506-04-118 on the packaging. These screws were sold by Encore Medical for shoulder replacements.
Look for the model number 506-04-118 on the packaging to confirm if it's the recalled item.
The packaging labels for these screws show a different size than the actual product, which could lead to improper installation during shoulder replacements.
The recall record does not specify a remedy, so check the packaging for the model number 506-04-118 to confirm if it's affected.
The recall indicates a potential for improper use, but the record does not mention specific injury risks.
We’ve drafted a message you can send Encore Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2010-2025 — Encore Medical Encore Medical Hello, I own a Encore Medical that is covered by recall Z-2010-2025 from Encore Medical. 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.
