Physio-control, Inc. - 3015876
FDA adverse event reports naming Physio-control, Inc. - 3015876 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PHYSIO-CONTROL, INC. - 3015876.
- Total reports
- 21,766
- Deaths
- 250
- Injuries
- 66
- Malfunctions
- 21,450
Reports per year
3912
513
414
1515
2416
7917
2,05318
2,08319
2,04620
2,49921
2,78622
2,45223
3,53824
2,78125
1,33326
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Automated External Defibrillators (Non-Wearable)MKJ21,618
- Electrode, ElectrocardiographDRX50
- Compressor, Cardiac, ExternalDRM45
- Dc-Defibrillator, Low-Energy, (Including Paddles)LDD22
- Electrode, Electrocardiograph, Multi-FunctionMLN19
- Over-The-Counter Automated External DefibrillatorNSA10
- Cable, ElectrodeIKD1
- TympanometerNAS1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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