Medtronic recalls 8 LINQ II Insertable Cardiac Monitors that may lose functionality due to moisture ingress. Affected devices have specific serial numbers and GTINs.
Devices may lose functionality due to susceptibility to moisture ingress.
Medtronic is recalling 8 LINQ II Insertable Cardiac Monitors that could lose functionality if exposed to moisture. This risk is serious for patients relying on the device for heart health monitoring.
The device may lose functionality due to moisture entering it, which could disrupt heart monitoring. This risk is particularly concerning for patients who rely on the device for critical health data.
Patients with Medtronic LINQ II Insertable Cardiac Monitors are affected. Those with the specific serial numbers listed in the recall are most at risk.
Check if your LINQ II Insertable Cardiac Monitor has one of the 8 specific serial numbers listed in the recall. The devices have unique GTINs associated with each serial number.
Verify your LINQ II Insertable Cardiac Monitor's serial number against the list of 8 affected devices provided in the recall.
8 devices with specific serial numbers and GTINs are being recalled.
The devices may lose functionality due to moisture ingress, which could disrupt heart monitoring.
No, but you should check if your device is affected and contact Medtronic if you have one of the listed serial numbers.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0782-2022 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0782-2022 from Medtronic. 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.
