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FDA (Device enforcement)Recalled 2014-09-02closedclass ii

Aerogen Ltd.: The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients o

Is my product affected?

The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb Professional Nebulizer System i

  • UPC 9144140519057
  • UPC 9144140616062
  • UPC 9144140702155
  • UPC 9144140710034
  • UPC 9125140522116
  • UPC 9125140526101
  • UPC 9125140527077
  • UPC 9125140609002
  • UPC 9125140609007
  • UPC 9125140616064
  • UPC 9125140627057
  • UPC 9125140702166
  • UPC 9125140710031
  • UPC 9125140805010
  • UPC 9125140805134
  • UPC 9122140520089
  • UPC 9122140521089
  • UPC 9122140528119
  • UPC 9122140609041
  • UPC 9122140626100
  • UPC 9122140728097
  • UPC 9122140730088
  • UPC 9124140609011
  • UPC 9124140620092
  • UPC 9124140623091
  • UPC 9123140521074
  • UPC 9123140610023
  • UPC 9123140710033
  • UPC 9123140724097
  • UPC 9120140519028
  • UPC 9120140519061
  • UPC 9120140526111
  • UPC 9120140630135
  • UPC 9120140701144
  • UPC 9120140702156
  • UPC 9120140714044
  • UPC 9121140521090
  • UPC 9121140522091
  • UPC 9121140522093
  • UPC 9121140523094

Check against the official notice below — it lists the full affected range.

What happened

Aerogen Ltd. is recalling approximately 1,223 power adapters manufactured by FRIWO GmbH (Model Number GPP10) used in Aeroneb Solo and Pro Nebulizer systems. The company received a small number of complaints reporting that the power adapter cover broke and became dislodged from the body of the adapter before use. The affected adapters were distributed worldwide, including across the United States and numerous international locations, and are associated with multiple Aeroneb nebulizer system models with specific lot numbers.

The recall source does not specify a remedy or corrective action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

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.

Details from the source

Reason for recall: 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. Distribution: Worldwide Distribution-USA (nationwide) including the states of CA, GA, IL, MS, NC, and TX, and the countries of Australia, Belgium, Canada, China, Czech Republic, Denmark, Egypt, Finland, France, Germany, Hungary, India, Ireland, Israel, Italy, Kuwait, Libya, Malaysia, Netherlands, Norway, Poland, Qatar, Russia, South Korea, Singapore, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, Quantity: 1,223 power adapters Lot/code info: FRIWO AC/DC Adapter Model Number: GPP10; The FRIWO AC/DC Adapter is supplied with the following Aeroneb Nebulizer systems and their respective model numbers: 1) Model Number: AG-AS3000-AU; Lot Numbers: 9144140519057 , 9144140616062 , 9144140702155 , 9144140710034; 2) Model Number: AG-AS3000-IN; Lot Numbers: 9125140522116 , 9125140526101 , 9125140527077 , 9125140609002 , 9125140609007 , 9125140616064 , 9125140627057 , 9125140702166 , 9125140710031 , 9125140805010 , 9125140805134; 3) Model Number: AG-AS3000-NE; Lot Numbers: 9122140520089 , 9122140521089 , 9122140528119 , 9122140609041 , 9122140626100 , 9122140728097 , 9122140730088; 4) Model Number: AG-AS3000-SC; Lot Numbers: 9124140609011 , 9124140620092 , 9124140623091; 5) Model Number: AG-AS3000-SE; Lot Numbers: 9123140521074 , 9123140610023 , 9123140710033 , 9123140724097; 6) Model Number: AG-AS3000-UK; Lot Numbers: 9120140519028 , 9120140519061 , 9120140526111 , 9120140630135 , 9120140701144 , 9120140702156 , 9120140714044; 7) Model Number: AG-AS3000-US; Lot Numbers: 9121140521090 , 9121140522091 , 9121140522093 , 9121140523094 , 9121140613066 , 9121140630138 , 9121140707023 , 9121140709030; 8) Model Number: AG-PX1000-IN; Lot Numbers: 9133140704002; 9) Model Number: ; Lot Numbers: ; 10) Model Number: AG-PX1000-NE; Lot Numbers: 9130140528119 , 9130140616060 , 9130140730040; 11) Model Number: AG-PX1000-SC; Lot Numbers: 9132140519072 , 9132140526107; 12) Model Number: AG-PX1000-SE; Lot Numbers: 9131140623154; 13) Model Number

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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