Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to Electroneurodiagnostic medical device may contain a defective printed...
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 Cadwell Industries Inc directly.
Affected Products
Cascade IOMAX Cortical Module, REF: 190296-200
Quantity: 26 units
Why Was This Recalled?
Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
Where Was This Sold?
This product was distributed to 2 states: CA, IL
About Cadwell Industries Inc
Cadwell Industries Inc has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report