Compressor, Air, Portable
Anesthesiology · 21 CFR 868.6250
Recent MDR events
5,408 adverse event reports on file
- MedlineJul 31, 2026MalfunctionMedline Industries, Lp1417592-2026-08096
- MedlineJul 31, 2026MalfunctionMedline Industries, Lp1417592-2026-08095
- MedlineJul 31, 2026MalfunctionMedline Industries, Lp1417592-2026-08094
- MedlineJul 31, 2026MalfunctionMedline Industries, Lp1417592-2026-08107
- MedlineJul 30, 2026MalfunctionMedline Industries, Lp1417592-2026-08054
- MedlineJul 30, 2026MalfunctionMedline Industries, Lp1417592-2026-08055
- MedlineJul 30, 2026MalfunctionMedline Industries, Lp1417592-2026-08098
- medlineJul 30, 2026MalfunctionMedline Industries, Lp1417592-2026-08097
- MedlineJul 29, 2026MalfunctionMedline Industries, Lp1417592-2026-07957
- MedlineJul 29, 2026MalfunctionMedline Industries, Lp1417592-2026-07958
Event type breakdown
Recalls
5 recall events for this product code
- Datex-Ohmeda, Inc.Open, ClassifiedJan 30, 2024
EVair air compressor, model numbers: M1230849 and M1230847
GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstrm Carestation/Pro ventilators, respectively. These elevated results were observed in preliminary testing that was conducted at an elevated room temperature of 40oC (104oF), at the lowest possible flow condition of 2 L/min (worstcase, minimum bias flow with no additional ventilation), and all of the gas being supplied from the compressor (i.e., FiO2 of 21% / no supplemental oxygen). GE HealthCare is continuing to evaluate the root cause for these elevated levels of formaldehyde. While these test conditions are not representative of typical clinical use conditions,GE HealthCare is taking this action to further reduce the potential for patient exposure.
Z-0774-2024 · View FDA record ↗ - Datex-Ohmeda, Inc.Open, ClassifiedJan 30, 2024
EVair 03 (Jun-air) air compressor, model numbers: 1609000 and 1609002
GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstrm Carestation/Pro ventilators, respectively. These elevated results were observed in preliminary testing that was conducted at an elevated room temperature of 40oC (104oF), at the lowest possible flow condition of 2 L/min (worstcase, minimum bias flow with no additional ventilation), and all of the gas being supplied from the compressor (i.e., FiO2 of 21% / no supplemental oxygen). GE HealthCare is continuing to evaluate the root cause for these elevated levels of formaldehyde. While these test conditions are not representative of typical clinical use conditions,GE HealthCare is taking this action to further reduce the potential for patient exposure.
Z-0775-2024 · View FDA record ↗ - Datex-Ohmeda, Inc.Open, ClassifiedJan 30, 2024
EvAir CPRSR Kit Upgrade:
GE HealthCare has become aware of elevated levels of formaldehyde when the EVair or EVair 03 (Jun-Air) optional compressors are used with the CARESCAPE R860 or Engstrm Carestation/Pro ventilators, respectively. These elevated results were observed in preliminary testing that was conducted at an elevated room temperature of 40oC (104oF), at the lowest possible flow condition of 2 L/min (worstcase, minimum bias flow with no additional ventilation), and all of the gas being supplied from the compressor (i.e., FiO2 of 21% / no supplemental oxygen). GE HealthCare is continuing to evaluate the root cause for these elevated levels of formaldehyde. While these test conditions are not representative of typical clinical use conditions,GE HealthCare is taking this action to further reduce the potential for patient exposure.
Z-0776-2024 · View FDA record ↗ - Maquet Cardiovascular Us Sales, LlcTerminatedJan 28, 2014
Compressor Mini
Maquet Compressor Mini may deliver compressed air at a temperature higher than specified.
Z-0848-2014 · View FDA record ↗ - Draeger Medical, Inc.TerminatedApr 5, 2007
Medical Air Compressor
Compressors not providing sufficient supply pressure to connected medical ventilator
Z-0674-2007 · View FDA record ↗
Registered firms
93 firms currently registered for this product code
Asia Connection Co., Ltd.
New Taipei City, TW
Nantong Kangjinchen Medical Equipment Co., Ltd.
Nantong Jiangsu, CN
Beijing Aeonmed Co., Ltd.
Sanhe Hebei, CN
Ceva Logistics Netherlands Bv (venray)
Oostrum Limburgh, NL
Boen Healthcare Co., Ltd.
Suzhou Jiangsu, CN
Covidien
- Galway, IE
Vega Technologies Inc.
Dongguan City Guangdong, CN
Besmed Health Business Corporation
New Taipei City, TW
Kitron Ab
Jonkoping, SE
Precision Medical, Inc.
NORTHAMPTON, PA, US
Javid De Mexico S. De R.l. De C.v. (resplabs)
Nogales Sonora, MX
Lifeport, Llc.
Woodland, WA, US
Oricare Inc.
Quakertown, PA, US
Drive Devilbiss Healthcare
Dayton, NJ, US
Devilbiss Healthcare Llc.
SOMERSET, PA, US
Venture Corporation Limited
Singapore North East, SG
Nidek Medical Products, Inc.
Birmingham, AL, US
Allied Medical Llc
Earth City, MO, US
P Bhogilal Pvt Ltd
Kolkata West Bengal, IN
Emg Technology Co., Ltd.
Taichung City, TW
Honsun (nantong) Co., Ltd.
Nantong Jiangsu, CN
Bi-rich Medical Devices (cambodia) Co. Ltd
BAVET Svay Rieng, KH
Pari Respiratory Equipment, Inc.
MIDLOTHIAN, VA, US
Drive Northpoint, Llc
Palmetto, GA, US
510(k) clearances
74 clearances for this product code
- Trudell Medical Intl.Oct 24, 2013
K131881 · OMBRA TABLE TOP COMPRESSOR
- Oricare, Inc.Aug 10, 2012
K113338 · MEDICAL AIR COMPRESSOR
- Ekom S.R.O.Oct 23, 2009
K091871 · DK50 DS
- Emg Technology Co., Ltd.Nov 19, 2008
K072634 · EMG TRITON -COMP,MODEL NCA01-XXX SERIES
- Ekom S.R.O.Oct 3, 2006
K060781 · MEDICAL COMPRESSOR, MODELS DK50 D AND DM
- Precision Medical, Inc.Dec 9, 2005
K051691 · MINIMATE COMPRESSOR
- Hamilton Medical AGMar 14, 2005
K041781 · VENTILAIR II MEDICAL AIR COMPRESSOR
- Newport Medical InstrumentsDec 15, 2004
K041406 · NEWPORT C250 AIR COMPRESSOR MODEL C250