AutoPulseResuscitation SystemRecalls & reported problems across all models
Zoll Circulation, Inc. · 46 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5,067
- Deaths reported
- 1
- Injuries reported
- 25
- Recalls
- 0
We found 46 models of AutoPulseResuscitation System by Zoll Circulation, Inc. in the FDA's device registry (GUDID). Together they are named in 5,067 adverse event reports in the FDA's MAUDE database, received between Aug 11, 2015 and Sep 30, 2026 — classified as 1 death, 25 injuries, 5,040 malfunctions.
The most frequently reported specific device problem is “Visual Prompts will not Clear” (3,503 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported AutoPulseResuscitation System problems
Device problems
- Visual Prompts will not Clear3,503
- Device Displays Incorrect Message775
- Device Operational Issue612
- Use of Device Problem608
- Device Operates Differently Than Expected289
- Failure to Power Up150
- No Display/Image139
- Display or Visual Feedback Problem131
Patient problems
- No Clinical Signs, Symptoms or Conditions2,125
- No Patient Involvement1,271
- Insufficient Information623
- No Known Impact Or Consequence To Patient521
- No Consequences Or Impact To Patient505
- No Information19
- Cardiac Arrest15
- Injury14
AutoPulseResuscitation System models
46 models, most reported first. Each model has its own page with its reports, recalls and device details.
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External3,208 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External317 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External276 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External250 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External241 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External189 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 death110 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External97 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External54 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External47 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External46 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External36 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External21 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External16 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External15 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External14 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External11 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External11 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External10 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External10 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External9 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External7 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External7 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External6 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External6 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External6 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External6 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External6 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External5 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External4 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External3 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External3 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External3 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External2 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External2 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External2 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External2 reports
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
- AutoPulse®Resuscitation System 100Compressor, Cardiac, External1 report
Recent AutoPulseResuscitation System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Use of Device Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954689 ↗MalfunctionSep 30, 2026Use of Device Problem; Noise, Audible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954588 ↗MalfunctionSep 30, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953108 ↗MalfunctionSep 30, 2026Display Difficult to Read
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952397 ↗MalfunctionSep 28, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50925258 ↗MalfunctionSep 25, 2026Output Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50903840 ↗MalfunctionSep 24, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50891792 ↗MalfunctionSep 23, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875958 ↗MalfunctionSep 23, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875699 ↗MalfunctionSep 23, 2026Use of Device Problem; Noise, Audible
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875465 ↗MalfunctionSep 23, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50874965 ↗MalfunctionSep 23, 2026No Display/Image; Noise, Audible
During device check, the AutoPulse Platform (SN (b)(6)) LCD failed to display data and generated a clicking sound when the LifeBand was connected. The AutoPulse Platform failed to operate. No patient involvement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869923 ↗MalfunctionSep 21, 2026Visual Prompts will not Clear
The AutoPulse Platform (SN (b)(6)) was deployed to resuscitate a patient. After the first compression cycle, the Platform displayed User Advisory 45 (Not at "Home" Position After Power-On/Restart). The customer attempted to clear the UA, but it persisted. Manual CPR was performed for the remainder of the call. No consequences or impacts on the patient.ZOLL tech support provided the customer with instructions on how to clear UA45 by rotating the drive shaft to the home position. ZOLL tech support has asked the customer to follow the instructions to clear the UA. Based on the additional information received, the AutoPulse Platform will be returned to ZOLL for evaluation.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50842499 ↗MalfunctionSep 18, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50812805 ↗MalfunctionSep 16, 2026Visual Prompts will not Clear
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50782503 ↗
Other Zoll Circulation, Inc. products
All Zoll Circulation, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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