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 Model 866120 Recalled by Invivo Corporation Due to During production, excess metal (aluminum) debris was found...
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 Model 866120
Quantity: 10 units
Why Was This Recalled?
During production, excess metal (aluminum) debris was found stuck to the cling plastic that covers the device's pole assembly. The metallic debris could affect system performance due to the potential for a failure to power up or loss of power. This could result in the loss of monitoring and a delay in diagnosis of the patient.
Where Was This Sold?
This product was distributed to 1 state: CA
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