AutoPulse®Resuscitation System 100 (REF 8700-0740-29)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 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00849111001250), received between Oct 20, 2016 and Jan 15, 2024 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Visual Prompts will not Clear” (5 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Visual Prompts will not Clear5
- No Display/Image1
Patient problems
- No Patient Involvement4
- Insufficient Information2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 15, 2024Visual Prompts will not Clear; Visual Prompts will not Clear
THE CUSTOMER REPORTED THE AUTOPULSE PLATFORM SN (B)(6) DISPLAYS FAULT 41 (PATIENT TEMPERATURE SENSOR FAILURE) MESSAGE THAN CANNOT BE CLEARED. IT IS UNKNOWN WHEN THE PROBLEM OCCURRED. HOWEVER, PATIENT USE INFORMATION WAS REQUESTED BUT NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Insufficient Information
MAUDE report 18511124 ↗MalfunctionJan 12, 2024Visual Prompts will not Clear; Visual Prompts will not Clear
AS REPORTED, THE AUTOPULSE PLATFORM (SN (B)(4), DISPLAYED A 'SYSTEM ERROR, OUT OF SERVICE, REVERT TO MANUAL CPR' ERROR MESSAGE". IT IS UNKNOWN WHEN THE PROBLEM OCCURRED. HOWEVER, PATIENT USE INFORMATION WAS REQUESTED BUT NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Insufficient Information
MAUDE report 18509199 ↗MalfunctionJan 30, 2020Visual Prompts will not Clear; Visual Prompts will not Clear
DURING PREVENTIVE MAINTENANCE ON JANUARY 9, 2020, THE RETURNED AUTOPULSE PLATFORM (SERIAL #(B)(4)) DISPLAYED "SYSTEM ERROR, OUT OF SERVICE, REVERT TO MANUAL CPR " DURING FUNCTIONAL TEST.
Patient problems: No Patient Involvement
MAUDE report 9648345 ↗MalfunctionJan 29, 2020Visual Prompts will not Clear; Visual Prompts will not Clear
DURING PREVENTIVE MAINTENANCE ON JANUARY 8, 2020, THE RETURNED AUTOPULSE PLATFORM (SERIAL #(B)(4)) DISPLAYED "SYSTEM ERROR, OUT OF SERVICE, REVERT TO MANUAL CPR " DURING FUNCTIONAL TEST.
Patient problems: No Patient Involvement
MAUDE report 9645155 ↗MalfunctionJan 29, 2020Visual Prompts will not Clear; Visual Prompts will not Clear
DURING PREVENTIVE MAINTENANCE ON (B)(6) 2020, THE RETURNED AUTOPULSE PLATFORM (SERIAL #(B)(4)) DISPLAYED "SYSTEM ERROR, OUT OF SERVICE, REVERT TO MANUAL CPR " DURING FUNCTIONAL TEST.
Patient problems: No Patient Involvement
MAUDE report 9645154 ↗MalfunctionOct 20, 2016No Display/Image; No Display/Image
IT WAS REPORTED THAT DURING AN EVALUATION OF THE AUTOPULSE PLATFORM (S/N (B)(4) PRIOR TO USE THE DEVICE SHOWED MISSING PIXELS IN THE PLATFORM DISPLAY SCREEN. NO PATIENT INVOLVED DURING THIS EVENT. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Patient Involvement
MAUDE report 6045612 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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