Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging Recalled by Ziehm Imaging Inc Due to Engineering change in 2006 resulted in a minor...
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 Ziehm Imaging Inc directly.
Affected Products
Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Quantity: 60 devices
Why Was This Recalled?
Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ziehm Imaging Inc
Ziehm Imaging Inc has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report