ZOLL AutoPulse NXT Resuscitation System May Stop Chest Compressions
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.
Use caution until it’s fixed
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/52684-zoll-autopulse-nxt-resuscitation-system-may-stop-chest-compressions.
Source Summary by GovInfoNow · govinfonow.com/recall/52684-zoll-autopulse-nxt-resuscitation-system-may-stop-chest-compressions · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1533-2025
Cite this page
“ZOLL AutoPulse NXT Resuscitation System May Stop Chest Compressions.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52684-zoll-autopulse-nxt-resuscitation-system-may-stop-chest-compressions. Based on FDA recall #Z-1533-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1533-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
The AutoPulse NXT Platform Model 200 with software version 2.0.1. Affected units have specific serial numbers listed in the recall notice.
- Brand
ZOLL- Product
Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200- Category
Medical device
What to do — step by step
Check Device Software Version
Verify the software version is 2.0.1 on the device display. If it is, the device may be affected.
Contact ZOLL for Guidance
Reach out to ZOLL directly for specific instructions on whether your device is affected and what to do next.
Where it went and when
Where it was distributed
Distributed in 19 states, and outside the U.S.
FDA distribution: “US: AL, CA, CT, FL, IL, KS, LA, MN, MO, MT, NC, ND, NM, NY, OH, OK< PA, TX, WI OUS: Canada, Hong Kong,” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, California, Connecticut, Florida, Illinois, Kansas, Louisiana, Minnesota, Missouri, Montana, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Texas, Wisconsin.
Recall timeline
FDA published this recall 50 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1533-2025 (March 4, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1533-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.