Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Recalled by DIXI MEDICAL USA Due to Potential deformation of the internal packaging (blister pack)...
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 DIXI MEDICAL USA directly.
Affected Products
The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length varying from 16 mm to 80.5 mm according to the electrode reference. Microdeep Depth Electrodes are intended for temporary use with recording, monitoring and stimulation equipment for the recording, monitoring and stimulation of electrical signals at the subsurface level of the brain.
Quantity: 484 units
Why Was This Recalled?
Potential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About DIXI MEDICAL USA
DIXI MEDICAL USA has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report