Corin Medical recalls Apex Knee System models KC-50090 to KC-55243 due to potential nylon packaging pouches losing integrity. Affected users should check their product details.
Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.
Corin Medical is recalling several models of the Apex Knee System because the nylon packaging material may have lost integrity over time. This could lead to pouches becoming weak or damaged, though the recall does not indicate immediate safety risks to users.
The nylon packaging material has aged and lost integrity, which may cause pouches to become weak or damaged. This could potentially lead to pouches failing during use, though the recall does not specify how this would impact the device's function.
Users of the Apex Knee System with model numbers KC-50090 through KC-55243 are affected. Patients receiving the device for knee surgery are most at risk if pouches become compromised.
Check the model number on the packaging or device label. The affected models range from KC-50090 to KC-55243, with specific serial numbers listed in the recall notice.
Review the model number and serial numbers listed in the recall to determine if your device is affected.
The recall states that the nylon packaging may have lost integrity, but it does not indicate immediate safety risks to users.
Check the model number and serial numbers against the list provided in the recall notice.
The recall does not specify a remedy, so users should check the product details and contact Corin Medical for further guidance.
We’ve drafted a message you can send Corin Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2069-2025 — Corin Medical Corin Medical Hello, I own a Corin Medical that is covered by recall Z-2069-2025 from Corin 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.
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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.
