AutoPulse Li-ion Battery™ 100 (REF 8700-0752-15)Recalls & reported problems
Zoll Circulation, Inc. · Box containing a Lithium Ion (Li-Ion) battery for use with the AutoPulse ® Platform. · Class 2
All models of AutoPulse Li-ion Battery (9)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00849111001915), received between Jun 30, 2022 and Jun 3, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Battery Problem” (2 reports).
1 other recall cover devices cleared under the same FDA submission (K112998); they may or may not involve this specific model.
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
- Battery Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 3, 2024Battery Problem; Battery Problem
THE CUSTOMER REPORTED THAT AFTER 30 MINUTES OF PLACING THE AUTOPULSE LI-ION BATTERY (SN (B)(6)) INTO THE AUTOPULSE MULTI-CHEMISTRY BATTERY CHARGER (MCC) (SN (B)(6)) FOR CHARGING, THE BATTERY WAS DAMAGED WITH TWO PENETRATING HOLES. THE BATTERY'S STATUS LEDS SHOWED NO LIGHTS. SMOKE BLACKENED THE LEFT BAY OF THE MCC. BESIDES SMOKE TRACES, THE MCC HAD NO DAMAGE AND FUNCTIONED AS INTENDED. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19448858 ↗MalfunctionJun 30, 2022Battery Problem; Battery Problem
DURING THE SHIFT CHECK, THE FULLY CHARGED AUTOPULSE LI-ION BATTERY (SN 10997) WILL NOT POWER ON THE AUTOPULSE PLATFORM. THE STATUS INDICATOR OF THE BATTERY SHOWED FOUR GREEN LIGHTS, INDICATING THAT THE BATTERY IS FULLY CHARGED. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14871062 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K112998. One submission often covers many models, so check the product and lot details in each record.
- Z-0118-2023 · Sep 22, 2022 · Open, ClassifiedAutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR
Other Compressor, Cardiac, External devices
- AutoPulse®Resuscitation System 100Zoll Circulation, Inc. · Compressor, Cardiac, External3,208 reports
- AutoPulse Li-ion Battery™ 100Zoll Circulation, Inc. · Compressor, Cardiac, External1,151 reports
- AutoPulse® Resuscitation System 100Zoll Circulation, Inc. · Compressor, Cardiac, External1,136 reports
- AutoPulse®Resuscitation System 100Zoll Circulation, Inc. · Compressor, Cardiac, External317 reports
- AutoPulse®Resuscitation System 100Zoll Circulation, Inc. · Compressor, Cardiac, External276 reports
- AutoPulse®Resuscitation System 100Zoll Circulation, Inc. · Compressor, Cardiac, External250 reports
- AutoPulse®Resuscitation System 100Zoll Circulation, Inc. · Compressor, Cardiac, External241 reports
- LUCAS 99576Jolife AB · Compressor, cardiac, external2 recalls9 deaths99 reports
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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