Reported Sep 28, 2016 · Terminated

Philips Expression Information Portal (IP5) Model 865471. The IP5 is intended to be used as a secondary display control…

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 Ste 200 · Orlando, FL · 32826-3286

Is this the product you have?

  • Philips Expression Information Portal (IP5) Model 865471. The IP5 is intended to be used as a secondary display control unit for the Expression MRI Patient Monitoring System and the Expression MR200 MRI Patient Monitoring System.
Lot codes and dates
  • 639 of 639 codes

    • Serial numbers US23200121
    • US23200122
    • US23200123
    • US23200124
    • US23200125
    • US23200126
    • US23200127
    • US23200128
    • US23200129
    • US23200130
    • US23200131
    • US23200132
    • US23200133
    • US23200134
    • US23200135
    • US23200136
    • US23200137
    • US23200138
    • US23200139
    • US23200140
    • US23200141
    • US23200142
    • US23200143
    • US23200144
    • US23200145
    • US23200146
    • US23200147
    • US23200148
    • US23200149
    • US23200150
    • US23200151
    • US23200152
    • US23200153
    • US23200154
    • US23200155
    • US23200156
    • US23200157
    • US23200158
    • US23200159
    • US23200160
    • US23200161
    • US23200162
    • US23200163
    • US23200164
    • US23200165
    • US23200166
    • US23200167
    • US23200168
    • US23200169
    • US23200170
    • US23200172
    • US23200173
    • US23200176
    • US23200177
    • US23200178
    • US23200179
    • US23200180
    • US23200181
    • US23200182
    • US23200183
Amount recalled
639 units

Where it was sold

  • Nationwide

Why it was recalled

Frozen Display Numerics and Disabled Menu Keys after extended run time. This customer notification was sent August 22, 2014.

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 Dec 14, 2016 · Data as of Sep 19, 6:00 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.