Boston Scientific recalls ALTR:2 EL DR pacemakers (model S722) due to intermittent over-sensing of Minute Ventilation sensor signals, which may cause improper heart rhythm management.
Boston Scientific has received reports of intermittent over-sensing of the Minute Ventilation (MV) sensor signal with certain Boston Scientific pacemaker and cardiac resynchronization therapy pacemaker systems (pacemakers).
Boston Scientific is recalling ALTRUA 2 EL DR pacemakers (model S722) because they may sense ventilation signals incorrectly, potentially causing improper heart rhythm management. This could lead to health issues for users with pacemakers.
The pacemaker may incorrectly sense ventilation signals, leading to improper heart rhythm management. This could cause the device to malfunction and potentially affect heart function.
Owners of the ALTRUA 2 EL DR pacemaker model S722 are affected. Those with pacemakers or cardiac resynchronization therapy devices are most at risk.
Check if your pacemaker is labeled 'ALTRUA 2 EL DR' with model number S722. This model was sold by Boston Scientific.
Identify your pacemaker model to confirm if it is the recalled ALTRUA 2 EL DR model S722.
The recall is for potential improper heart rhythm management due to incorrect ventilation signal sensing, but the risk level is low.
Check your pacemaker model; if it matches the recalled model, contact Boston Scientific for further instructions.
Look for the model number S722 on your ALTRUA 2 EL DR pacemaker. This model was sold by Boston Scientific.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0364-2018 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0364-2018 from Boston Scientific. 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.
