COAPTIUM CONNECT medical device (model NCOCO1575) recalled due to unverified 36-month shelf life. Using beyond validated shelf life may cause device breakage requiring revision surgery.
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may result in perioperative breakage of the device rendering device unusable; worst-case outcome would be revision surgery.
COAPTIUM CONNECT nerve repair devices with model number NCOCO1575 are being recalled because their shelf life of 36 months isn't proven. Using these devices after this date could cause them to break during surgery, requiring additional procedures.
The device's shelf life of 36 months isn't supported by real-time data. If used beyond this period, the device may break during surgery, requiring a revision procedure.
Patients who received COAPTIUM CONNECT nerve repair devices with model NCOCO1575. The risk is highest for those using devices beyond the validated shelf life.
Check for model number NCOCO1575 on the device. Devices were sold with lot numbers 250700007, 251000031, and 260300041.
Verify the device's current shelf life label; if it shows 36 months or older, it may need replacement.
The 36-month shelf life isn't substantiated by real-time data. Using beyond this date may cause device breakage during surgery.
The worst-case outcome is a revision surgery to replace the device.
Look for model number NCOCO1575 with lot numbers 250700007, 251000031, or 260300041.
We’ve drafted a message you can send COAPTIUM CONNECT to request your refund or repair — edit it as you like.
Subject: Recall Z-2902-2026 — COAPTIUM CONNECT COAPTIUM CONNECT Hello, I own a COAPTIUM CONNECT that is covered by recall Z-2902-2026 from COAPTIUM CONNECT. 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.
