Medtronic recalls LINQ II Model LNQ22 cardiac monitors that may fail to detect critical heart episodes after a reset. Owners should contact Medtronic for guidance.
Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's after a ride-through POR reset.
Medtronic is recalling LINQ II Model LNQ22 insertable cardiac monitors that may fail to detect critical heart episodes after a reset. This could lead to missed medical events and potential harm.
The device may fail to detect critical heart episodes like bradycardia, asystole, or premature ventricular contractions after a reset. This could result in missed medical events and potential harm.
Patients with Medtronic LINQ II Model LNQ22 cardiac monitors are affected. Those with heart conditions requiring continuous monitoring are at higher risk.
Check for the model number LNQ22 on the device. The product is an insertable cardiac monitor sold as sterile, EO Rx only.
Reach out to Medtronic for specific guidance on the recall and next steps.
The model number is LNQ22.
The device may fail to detect critical heart episodes like bradycardia, asystole, or premature ventricular contractions after a reset.
The recall does not specify an immediate stop; contact Medtronic for guidance.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2076-2021 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2076-2021 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.
