Reported Nov 20, 2013 · Terminated

SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage:…

Baxter Healthcare Corp.

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: Baxter Healthcare Corp. · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2
  • revision B) Product UsageIntended to be used as a visual aid during the controlled administration of intravenous fluids. These fluids may include pharmaceutical drugs, blood, blood products and mixtures of required patient therapy
Lot codes and dates
  • Product Code35700BAX & 35700ABB
  • Serial Numbers

    91 of 91 codes

    • 433713
    • 435563
    • 704056
    • 707290
    • 715315
    • 724216
    • 740127
    • 752318
    • 752447
    • 753675
    • 754947
    • 759766
    • 765934
    • 770034
    • 772017
    • 773470
    • 776507
    • 781016
    • 781969
    • 783352
    • 783454
    • 787567
    • 789720
    • 791225
    • 794828
    • 794990
    • 797185
    • 804798
    • 808393
    • 808764
    • 810971
    • 812076
    • 818718
    • 821213
    • 824067
    • 824198
    • 839143
    • 850028
    • 850577
    • 852007
    • 852431
    • 855450
    • 860201
    • 864799
    • 876765
    • 877548
    • 877944
    • 878637
    • 879810
    • 879886
    • 880022
    • 884707
    • 884778
    • 885565
    • 889416
    • 889814
    • 890949
    • 890987
    • 894957
    • 895413
Amount recalled
346 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

Baxter Healthcare Corporation is recalling the LCD display screen on the SIGMA SPECTRUM Infusion Pump with Master Drug Library for not meeting standards for withstanding an electrostatic discharge.

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

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 9, 2016 · Data as of Sep 19, 5:21 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.