Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F Recalled by Siemens Medical Solutions USA, Inc. Due to Due to adverse events received by the firm...
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 Siemens Medical Solutions USA, Inc. directly.
Affected Products
ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F
Quantity: N/A
Why Was This Recalled?
Due to adverse events received by the firm for left atrial perforations and Atrioventricular Node block.
Where Was This Sold?
This product was distributed to 19 states: AZ, CA, FL, GA, IL, KY, MA, MI, MN, NJ, NY, OH, OK, OR, PA, TX, VA, WA, WV
About Siemens Medical Solutions USA, Inc.
Siemens Medical Solutions USA, Inc. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report