Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular Recalled by Toshiba American Medical Systems Inc Due to The table base rotational brake that holds the...
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 Toshiba American Medical Systems Inc directly.
Affected Products
INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V series includes a floor mounted multi-axis positioner.
Quantity: 28 units
Why Was This Recalled?
The table base rotational brake that holds the table top may not always be engaged when any force or side impact is applied to the table top.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Toshiba American Medical Systems Inc
Toshiba American Medical Systems Inc has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report