Reported Oct 22, 2014 · Terminated

Philips Expression MR200 MRI Patient Monitoring System

Invivo Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Invivo Corporation · 12151 Research Pkwy · Orlando, FL · 32826-3222

Is this the product you have?

  • Philips Expression MR200 MRI Patient Monitoring System
Lot codes and dates
  • Model866120
  • Lot numbers
    • US33600004
    • US33600005
    • US33600006
    • US33600007
    • US33600008
    • US33600009
    • US33600010
    • US33600011
    • US33600012
    • US33600013
    • US33600014
    • US33600015
    • US33600016
    • US33600017
    • US33600018
    • US33600019
    • US33600020
    • US33600022
    • US33600023
    • US33600024
    • US33600025
    • US33600026
    • US33600027
    • US33600028
Amount recalled
24 units.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 12, 2017 · Data as of Sep 19, 6:15 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.