Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Atrium Express Dry Seal Chest Drain ATS Blood Recovery Recalled by Atrium Medical Corporation Due to Product that was previously recalled because the Chest...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Atrium Medical Corporation directly.
Affected Products
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
Quantity: 195 Cases; Total 1170 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 9 states: AK, CA, MD, MN, MO, NJ, NC, OH, UT
About Atrium Medical Corporation
Atrium Medical Corporation has 150 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report