ZOLL recalls AutoPulse NXT Platform Model 200 devices that may stop chest compressions during CPR due to software error FC1060. Affected units have specific serial numbers.
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
ZOLL is recalling AutoPulse NXT Resuscitation System Model 200 devices because they may stop chest compressions during CPR due to a software error. This could lead to inadequate resuscitation efforts if the device fails to function properly.
The device may stop chest compressions or fail to provide adequate compressions due to a software error (code FC1060). This could result in inadequate resuscitation efforts during critical cardiac emergencies.
Healthcare professionals using the AutoPulse NXT Platform Model 200 for CPR. Those most at risk are medical personnel who rely on this device during cardiac emergencies.
The AutoPulse NXT Platform Model 200 with software version 2.0.1. Affected units have specific serial numbers listed in the recall notice.
Verify the software version is 2.0.1 on the device display. If it is, the device may be affected.
Reach out to ZOLL directly for specific instructions on whether your device is affected and what to do next.
The device may stop chest compressions or fail to provide adequate compressions due to software error FC1060. It is not safe to use without verification.
Check for software version 2.0.1 and the specific serial numbers listed in the recall notice.
Contact ZOLL directly for guidance on whether your device is affected and what steps to take.
We’ve drafted a message you can send ZOLL to request your refund or repair — edit it as you like.
Subject: Recall Z-1533-2025 — ZOLL ZOLL Hello, I own a ZOLL that is covered by recall Z-1533-2025 from ZOLL. 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.
