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Atrium Medical Corporation recalls Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
Recalled July 9, 2014 · FDA recall Z-1959-2014 · Atrium Medical
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. · FDA Class II
Units
195 Cases; Total 1170 units
Sold at
Distributed in the states of AK, CA, MD, MN, MO, NC, NJ, OH, and UT.
Description
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.
Product
Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.
Manufacturer(s)
Atrium Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →