AutoPulse NXT Resuscitation System Model 200 (REF 8700-001017)Recalls & reported problems
Zoll Circulation, Inc. · Shoulder Restraint English · Class 2
All models of AutoPulse NXT Resuscitation System (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00849111003025), received between Dec 30, 2025 and Dec 30, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 30, 2025Use of Device Problem; Use of Device Problem
THE CUSTOMER REPORTED THEY WERE DISPATCHED TO A CARDIAC ARREST. THE AUTOPULSE NXT PLATFORM (SN (B)(6)) WAS APPLIED TO THE APPROXIMATELY 52-YEAR-OLD, 250-270-POUND MALE PATIENT AFTER SEVERAL MINUTES. THE MED UNIT BEGAN TRANSPORT TO THE PCI FACILITY. AFTER APPROXIMATELY 20 MINUTES, THE PLATFORM SUDDENLY STOPPED ON ITS OWN. NO ONE WAS TOUCHING THE CONTROLS AT THE TIME. ACCORDING TO THE CUSTOMER, NO WARNING LIGHTS WERE NOTED. THE GREEN START BUTTON WAS PRESSED AND THE PLATFORM RESUMED AS NORMAL. AFTER APPROXIMATELY 3 MINS, A BATTERY CHANGE OCCURRED, AND THE PLATFORM RESUMED NORMAL OPERATIONS. THERE IS NO SUSPECTED BATTERY MALFUNCTION. AFTER 3-5 MINUTES, THE NXT BAND (LOT UNKNOWN) RIPPED OFF THE PATIENT. THE CREW CONTINUED WITH MANUAL CPR AND THE NXT BAND WAS ATTEMPTED TO BE REATTACHED UNSUCCESSFULLY. THE PATIENT WAS KEPT ON THE PLATFORM BUT THERE WERE NO FURTHER ATTEMPTS TO USE THE PLATFORM. MANUAL CPR WAS PERFORMED UNTIL HAND OFF AT THE HOSPITAL. NO CONSEQUENCES OR IMPACT ON THE PATIENT. AFTER THE CALL WAS COMPLETED, INSPECTION OF THE NXT BAND FOUND THAT THE VELCRO RIPPED PARTIALLY OFF. THE BAND RIPPED/TORE MID-WAY BETWEEN THE CONNECTION TO BOARD AND LARGEST PART OF THE BAND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23930688 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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