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Draeger Medical Recalls
78 recalls on record · March 20, 2013 to December 25, 2024 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 25, 2024Medical DevicesFDA
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstatio
Hazard: The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
December 25, 2024Medical DevicesFDA
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A300 Model/Catalog Number: 8211300 The Atlan is an anesthesia workstation
Hazard: The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
November 20, 2024Medical DevicesFDA
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Componen
Hazard: The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
November 20, 2024Medical DevicesFDA
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component:
Hazard: The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
April 24, 2024Medical DevicesFDA
Draeger Medical, Inc. recalls Dr¿ger Perseus A500 Anesthesia Workstation
Hazard: Unexpected shutdown while operating on battery power.
August 30, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Carina Sub-Acute Care Ventilator
Hazard: Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients.
July 19, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Oxylog 3000 Plus emergency and transport ventilator
Hazard: Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Anesthesia Circuit Kit Coax HEPA, MP17102
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Set2Go Ventilation 12 (A), MP07968
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Anesthesia Set Coax 180, MP03384
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Ventstar Coax 230, MP03376
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls ID Coax 180, MP03375
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Ventstar Coax 180, MP03374
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Ventstar Coax, MP03373
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Anesthesia Circuit Kit Coax 3, MP02732
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Anesthesia Circuit Kit Coax 1, MP02730
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Coax (P) 150, MP00379
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Bag Set (N) 110, MP00383
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Watertrap (N) 180, MP00363
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Basic (N) 180, MP00353
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Anesthesia (N) 180, MP00333
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls ID Circuit Basic (P) 180, MP01340
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar breathing bag Set (P) 110, MP00384
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Anesthesia WT (P)180, MP00374
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Watertrap (P) 180 w/oLL, MP00362
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Watertrap (P) 180, MP00361
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Basic (P)250, MP00352
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls VentStar Basic (P)180, MP00351
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
May 24, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls Seattle PAP Plus, MP02260
Hazard: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
March 1, 2023Medical DevicesFDA
Draeger Medical, Inc. recalls NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)
Hazard: The magnets used in the swivel frame/tube set and the headgear clips might impact medical devices (implanted as well as not implanted) and metallic implants.