Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Expression MR200 MRI Patient Monitoring System. Recalled by Invivo Corporation Due to The MR 200 devices failed the initial power...
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 Invivo Corporation directly.
Affected Products
Philips Expression MR200 MRI Patient Monitoring System.
Quantity: 20
Why Was This Recalled?
The MR 200 devices failed the initial power up test due to capacitor short and hi-pot testing; possible loss of Patient Monitoring or User/Service Electrical Shock.
Where Was This Sold?
This product was distributed to 11 states: CA, FL, IN, KY, MN, NJ, NY, NC, OK, SD, TX
About Invivo Corporation
Invivo Corporation has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report