FDAFDA · Food and drugs·Recall number Z-0741-2014
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.
Published January 22, 2014 · Recall initiated: November 19, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Chest Drain tubing of of the ATS Blood recovery may leak or disconnect
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Atrium Medical Corporation
- Distributor
- Worldwide Distribution-USA (nationwide) and the countries of Australia, Canada, Austria, Ireland, Romania, South Africa, Colombia, Lebanon Netherlands, Jordan, Russia, and Taiwan.
- Lot
- Lot number starting with 10883097 and the ending lot number 10913346. All units in between and including these two numbers.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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