DJO SURGICAL recalls ALTIVATE REVERSE WEDGE GLENO: 804-06-310 due to potential binding during use. This may cause injury. Consumers should contact DJO SURGICAL for details.
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
DJO SURGICAL is recalling their ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE (model 804-06-310) because it may bind or kick during use, potentially causing injury. This is a safety issue for medical professionals using the device.
The reamer may bind or kick during use, which could cause injury to the user. This happens because the device might not move smoothly when being used in surgical procedures.
Medical professionals who use this surgical tool are most at risk. The recall affects all units sold with the model number 804-06-310.
Check for the model number 804-06-310 on the product. The product is made of stainless steel and cobalt-chromium alloy and is non-sterile.
Reach out to DJO SURGICAL for specific instructions on how to handle the recalled item.
The recall indicates a potential risk of binding during use, so it is not recommended to use this product without contacting DJO SURGICAL first.
Look for the model number 804-06-310 on the product. The product is made of stainless steel and cobalt-chromium alloy and is non-sterile.
Contact DJO SURGICAL for specific instructions on how to handle the recalled item.
We’ve drafted a message you can send DJO SURGICAL to request your refund or repair — edit it as you like.
Subject: Recall Z-2548-2025 — DJO SURGICAL DJO SURGICAL Hello, I own a DJO SURGICAL that is covered by recall Z-2548-2025 from DJO SURGICAL. 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.
