Exactech recalls specific models of Equinoxe Cage Glenoid implants due to potential mislabeling. Affected units include serial numbers 6132993-6133032. Consumers should check their product details.
The product may be mislabeled.
Exactech is recalling certain Equinoxe Cage Glenoid implants that may be mislabeled. This could lead to incorrect use in medical procedures, but the recall does not indicate immediate safety risks.
Mislabeled implants could be used in the wrong surgical procedure, potentially causing complications. However, the recall does not indicate that the mislabeling causes immediate injury or death.
Patients who received the specific Equinoxe Cage Glenoid implants with the listed serial numbers. Surgeons and medical staff using these implants are most at risk of incorrect labeling.
Check if your implant has the model 'Equinoxe Cage Glenoid, Posterior Augment, Right, Medium' and the listed serial numbers (6132993-6133032).
Verify your implant's serial number against the list of affected numbers provided in the recall.
No, the recall does not require stopping use. The issue is mislabeling, not a safety hazard.
Check your implant's serial number against the list of affected numbers provided in the recall.
The recall states the product may be mislabeled, but it does not indicate a risk of injury or serious harm.
We’ve drafted a message you can send Exactech to request your refund or repair — edit it as you like.
Subject: Recall Z-0460-2021 — Exactech Exactech Hello, I own a Exactech that is covered by recall Z-0460-2021 from Exactech. 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.
