Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due to GE Healthcare Surgery announces a voluntary field action...
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 9800. MDL Numbers: D222250, D141598
Quantity: 26,256 total
Why Was This Recalled?
GE Healthcare Surgery announces a voluntary field action for the OEC 9800 and OEC 9900 Elite due to additional supplementation to the user documentation to include areas for enhanced planned maintenance and component replacement frequencies.
Where Was This Sold?
This product was distributed to 1 state: VA
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