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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 8003140519057
  • UPC 8003140708015
  • UPC 8003140722089
  • UPC 800140731124
  • UPC 8000140520074
  • UPC 8000140520087
  • UPC 8000140530103
  • UPC 8000140619082
  • UPC 8000140620092
  • UPC 8000140624103
  • UPC 8000140624118
  • UPC 8000140701104
  • UPC 8000140702153
  • UPC 8000140721056
  • UPC 8000140726097
  • UPC 8000140728100
  • UPC 8000140728117
  • UPC 8000140728120
  • UPC 8000140625100
  • UPC 8000140624100
  • UPC 8001140519067
  • UPC 8001140624115
  • UPC 8001140714044
  • UPC 8001140728065
  • UPC 8001140731125
  • UPC 8002140520090
  • UPC 8002140521088
  • UPC 8002140522091
  • UPC 8002140522093
  • UPC 8002140523094
  • UPC 8002140523095
  • UPC 8002140526114
  • UPC 8002140527096
  • UPC 8002140603121
  • UPC 8002140603130
  • UPC 8002140613067
  • UPC 8002140613068
  • UPC 8002140616069
  • UPC 8002140616070
  • UPC 8002140626123

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

What happened

Aerogen Ltd. is recalling approximately 2,421 power adapters manufactured by FRIWO GmbH that are used with Aeroneb Solo and Pro Nebulizer systems. The company received a small number of complaints indicating that the power adapter cover had broken and separated from the adapter body before use. The affected adapters have been distributed worldwide, including throughout the United States and numerous international locations.

The recall involves specific model numbers and lot numbers of the FRIWO AC/DC Adapter Model Number GPP10 supplied with various Aeroneb Nebulizer Pro family systems. The source document does not specify a remedy or action that affected consumers should take.

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: 2,421 power adapters Lot/code info: FRIWO AC/DC Adapter Model Number: GPP10; The FRIWO AC/DC Adapter is supplied with the following Aeroneb Nebulizer Pro family of systems: and their respective model numbers: 1) Model Number: AG-AP1040-AU; Lot Numbers: 8003140519057 , 8003140708015 , 8003140722089 ; 2) Model Number: AG-AP1040-EU; Lot Numbers: 800140731124 , 8000140520074 , 8000140520087 , 8000140520087 , 8000140530103 , 8000140619082 , 8000140620092 , 8000140624103 , 8000140624118 , 8000140701104 , 8000140702153 , 8000140721056 , 8000140726097 , 8000140728100 , 8000140728117 , 8000140728120 , 8000140625100, 8000140624100; 3) Model Number: AG-AP1040-UK; Lot Numbers: 8001140519067 , 8001140624115 , 8001140714044 , 8001140728065 , 8001140731125; 4) Model Number: AG-AP1040-US; Lot Numbers: 8002140520090 , 8002140521088 , 8002140522091 , 8002140522093 , 8002140523094 , 8002140523095 , 8002140526114 , 8002140527096 , 8002140603121 , 8002140603130 , 8002140613067 , 8002140613068 , 8002140616069 , 8002140616070 , 8002140626123 , 8002140627124 , 8002140627125 , 8002140627138 , 8002140711036 , 8002140714042 , 8002140721085 , 8002140721087 , 8002140722091 , 8002140722092 , 8002140722093; 5) Model Number: AG-AP1500-IN; Lot Numbers: 9948140702153; 6) Model Number: AG-AP1500-UK; Lot Numbers: 9953140801132; 7) Model Number: AG-AP1500-US; Lot Numbers: 9939140522091 , 9939140630138; 8) Model Number: AG-AP6000(DG)-FR; Lot Numbers: 9998140611025; 9) Model Number: AG-AP6000(DG)-GE; Lot Numbers: 9997140611024; 10) Model Number: AG-

Source

Official record: FDA (Device enforcement) ↗

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

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