Reported Jan 15, 2014 · Terminated

SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)

GE Healthcare, LLC

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: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)
Lot codes and dates
  • Mfg Lot or Serial #

    2,169 of 2,169 codes

    • SA307140598GA
    • SA307140599GA
    • SA307140600GA
    • SA307140601GA
    • SA307140605GA
    • SA307140606GA
    • SA307140607GA
    • SA307140610GA
    • SA307140611GA
    • SA307140612GA
    • SA307140614GA
    • SA307140615GA
    • SA307140618GA
    • SA307140619GA
    • SA307140622GA
    • SA307140623GA
    • SA307140627GA
    • SA307140628GA
    • SA307140631GA
    • SA307140632GA
    • SA307140636GA
    • SA307140637GA
    • SA307140639GA
    • SA307140640GA
    • SA307140641GA
    • SA307140642GA
    • SA307140644GA
    • SA307150645GA
    • SA307150646GA
    • SA307150655GA
    • SA307150656GA
    • SA307020391GA
    • SA307030405GA
    • SA307030424GA
    • SA307070446GA
    • SA307070447GA
    • SA307070448GA
    • SA307080462GA
    • SA307080463GA
    • SA307080484GA
    • SA307080508GA
    • SA307080523GA
    • SA307110548GA
    • SA307110556GA
    • SA307110571GA
    • SA307190716GA
    • SA307190737GA
    • SA307190739GA
    • SA307190750GA
    • SA307190768GA
    • SA307020379GA
    • SA307020384GA
    • SA307020386GA
    • SA307030407GA
    • SA307030409GA
    • SA307030412GA
    • SA307030414GA
    • SA307060432GA
    • SA307070436GA
    • SA307070440GA
Amount recalled
17,444 (11,418 units US, 6,026 units OUS).

Where it was sold

Why it was recalled

GE Healthcare has recently become aware of a potential safety issue which affects all Patient Date Modules produced from April 2007 through June 2010, encompassing Fiscal Week 13, 2007 through 26, 2010 due to fluid ingress into the top cover assembly which can result in heat buildup.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new produce recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 19, 2016 · Data as of Sep 19, 6:12 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.