FDAFDA · Food and drugs·Recall number Z-1959-2014
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
Published July 9, 2014 · Recall initiated: April 28, 2014
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
Product that was previously recalled because the Chest Drain tubing of the ATS Blood recovery may leak or disconnect, was released for distribution in error.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Atrium Medical Corporation
- Distributor
- Distributed in the states of AK, CA, MD, MN, MO, NC, NJ, OH, and UT.
- Lot
- Lot Number: 10906458
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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