Class II — Potential Health Hazard

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 Failure to produce the Non-Invasive Blood Pressure (NIBP)...

Date: September 5, 2014
Company: Invivo Corporation
Status: Terminated
Source: FDA (Device)

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: 24 units.

Why Was This Recalled?

Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.

Where Was This Sold?

This product was distributed to 6 states: CA, GA, MI, NV, NJ, TX

Affected (6 states)Not affected

About Invivo Corporation

Invivo Corporation has 19 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report