DJO SURGICAL recalls FA S Altivate Reverse Glenoid Tray due to potential reamer binding during or before surgery, which could cause injury. Affected patients should contact the manufacturer 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 FA S Altivate Reverse Glenoid Tray surgical device because it may bind or kick during use, potentially causing injury. This recall affects surgeons and hospitals using the product for shoulder replacements.
The reamer may bind or kick during or immediately before surgery, which could cause injury to the patient. This happens because the device is designed for use in specific shoulder conditions but may not function properly under certain surgical conditions.
Surgeons and hospitals that use the FA S Altivate Reverse Glenoid Tray for shoulder replacements are most at risk. Patients who have undergone surgery with this device should consult their surgeon.
The product is a surgical device called the FA S Altivate Reverse Glenoid Tray made by DJO SURGICAL. It was sold for shoulder replacements and has no specific model or catalog number listed in the recall.
Reach out to DJO SURGICAL directly for information about the recall and next steps.
The recall states there is a potential for the reamer to bind or kick during use, which could cause injury. The product is not safe to use without addressing this risk.
The product is a surgical device called the FA S Altivate Reverse Glenoid Tray made by DJO SURGICAL. It has no specific model or catalog number listed in the recall.
Contact DJO SURGICAL directly for information about the recall and next steps.
We’ve drafted a message you can send DJO SURGICAL to request your refund or repair — edit it as you like.
Subject: Recall Z-2549-2025 — DJO SURGICAL DJO SURGICAL Hello, I own a DJO SURGICAL that is covered by recall Z-2549-2025 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.
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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.
