Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic Navigation Due to Medtronic Navigation is recalling certain components of the...
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 Medtronic Navigation directly.
Affected Products
PoleStar system (N20 / N30) Warning Lamps Control Box, Warning Lamps Control Box Cables, Thermoflex Chiller Product The PoleStar Surgical MRI System is intended for use as an intraoperative imaging device to produce MRI images of sections of the head selected by the physician.
Quantity: 52
Why Was This Recalled?
Medtronic Navigation is recalling certain components of the PoleStar system (N20 / N30) because of misplaced ground pins which may cause electrical shock to the user.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Navigation
Medtronic Navigation has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report