AutoPulse®Resuscitation System 100 (REF 8700-0730-08-66)Recalls & reported problems
Zoll Circulation, Inc. · The AutoPulse System consists of 4 primary components, a reusable Platform, a single use chest compression assembly (LifeBand), a rechargeable battery, and a battery charger. · Class 2
All models of AutoPulseResuscitation System (46)
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 00849111000796), received between Apr 16, 2020 and Apr 16, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Visual Prompts will not Clear” (1 report).
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.
Most reported problems
Device problems
- Visual Prompts will not Clear1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 16, 2020Visual Prompts will not Clear; Visual Prompts will not Clear
DURING USE OF THE LOANER AUTOPULSE PLATFORM (SN: (B)(4)), THE PLATFORM DISPLAYED THE FOLLOWING USER ADVISORIES: UA17 (MAX MOTOR ON TIME EXCEEDED DURING ACTIVE OPERATION), UA45 (NOT AT "HOME" POSITION AFTER POWER-ON/RESTART), AND UA02 (COMPRESSION TRACKING ERROR). THE CUSTOMER TRIED TO ADJUST THE LIFEBAND TO REMEDY THE OBSERVED USER ADVISORIES, BUT IT WAS UNSUCCESSFUL. ALSO, THE PLATFORM STOPPED COMPRESSIONS ALTHOUGH THE LCD WAS DISPLAYING THAT THE BATTERY ICON STATUS WAS AT 2/3 OF FULL CHARGE. UNKNOWN IF THE PLATFORM WAS USED ON A PATIENT OR NOT. HOWEVER, THERE IS NO REPORT OF CONSEQUENCES OR IMPACT TO PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9969368 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page