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Siemens Medical Solutions USA, Inc. recalls ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F
Recalled October 14, 2020 · FDA recall Z-0090-2021 · Siemens Medical Solutions USA
Hazard
Due to adverse events received by the firm for left atrial perforations and Atrioventricular Node block. · FDA Class II
Units
N/A
Sold at
U.S.: AZ, CA, FL, GA, IL, KY, MA, MI, MN, NJ, NY, OH, OK, OR, PA, TX, VA, WA and WV. O.U.S; Canada
Description
Due to adverse events received by the firm for left atrial perforations and Atrioventricular Node block.
Product
ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F
Manufacturer(s)
Siemens Medical Solutions USA, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →