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Aerogen Recalls

4 recalls on record · October 29, 2014 to October 29, 2014 · Medical Devices

October 29, 2014Medical DevicesFDA
Aerogen Ltd. recalls The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aero
Hazard: Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use.
October 29, 2014Medical DevicesFDA
Aerogen Ltd. recalls The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aero
Hazard: Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use.
October 29, 2014Medical DevicesFDA
Aerogen Ltd. recalls The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aero
Hazard: Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use.
October 29, 2014Medical DevicesFDA
Aerogen Ltd. recalls The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aero
Hazard: Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had broken and dislodged from the body of the adapter prior to use.
Aerogen Recalls | RecallWatchUSA