Devices

Device Recall Atrium Medical Oasis Dry Suction Water Seal ATS

  • Modèle / numéro de série
    Lot number starting with 10883097 and the ending lot number 10913346. All units in between and including these two numbers.
  • Classification du dispositif
    Anesthesiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) and the countries of Australia, Canada, Austria, Ireland, Romania, South Africa, Colombia, Lebanon Netherlands, Jordan, Russia, and Taiwan.
  • Description du dispositif
    Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain Dual patient lines; Product Code: 3652-100. || To evacuate air and/or fluid from the chest cavity or mediastinum.
  • Manufacturer
    Atrium Medical Corporation
  • 1 Event

Fabricant

Atrium Medical Corporation
  • Adresse du fabricant
    Atrium Medical Corporation, 5 Wentworth Dr, Hudson NH 03051-4929
  • Société-mère du fabricant (2017)
    Getinge AB
  • Source
    USFDA

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Device Recall Atrium Medical Oasis Dry Suction Water Seal ATS
  • Modèle / numéro de série
    Lot number starting with 10883097 and the ending lot number 10913346. (All units in between and including these two numbers)
  • Classification du dispositif
    Anesthesiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) and the countries of Australia, Canada, Austria, Ireland, Romania, South Africa, Colombia, Lebanon Netherlands, Jordan, Russia, and Taiwan.
  • Description du dispositif
    Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with in-line connectors Product Code: 3650-100. || To evacuate air and/or fluid from the chest cavity or mediastinum.
  • Manufacturer
    Atrium Medical Corporation