Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OEC Flexiview 8800 Systems with 9-inch Image Intensifier Recalled by GE OEC Medical Systems, Inc Due to Image intensifiers on systems, used to provide fluoroscopic/digital...
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 GE OEC Medical Systems, Inc directly.
Affected Products
OEC Flexiview 8800 Systems with 9-inch Image Intensifier
Quantity: 2
Why Was This Recalled?
Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion, bruise, pain.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE OEC Medical Systems, Inc
GE OEC Medical Systems, Inc has 48 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report