Reported Sep 28, 2016 · Terminated

LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician…

Hospira Inc.

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: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579

Is this the product you have?

  • LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.
Lot codes and dates
  • 2,716 of 2,716 codes

    • Serial Number 15553367
    • 16224548
    • 16224939
    • 16225091
    • 16225646
    • 16225851
    • 16226006
    • 16226095
    • 16226117
    • 16226159
    • 16226360
    • 16226383
    • 16226435
    • 16226460
    • 16226680
    • 16226707
    • 16226726
    • 16226730
    • 16226756
    • 16226763
    • 16226891
    • 16226895
    • 16226898
    • 16226910
    • 16226917
    • 16226918
    • 16226919
    • 16226920
    • 16226921
    • 16226922
    • 16226923
    • 16226924
    • 16226925
    • 16226926
    • 16226927
    • 16226928
    • 16226929
    • 16226930
    • 16226931
    • 16226932
    • 16226933
    • 16226934
    • 16226935
    • 16226936
    • 16226937
    • 16226938
    • 16226939
    • 16226940
    • 16226941
    • 16226943
    • 16226944
    • 16226945
    • 16226946
    • 16226947
    • 16226948
    • 16226949
    • 16226950
    • 16226951
    • 16226952
    • 16226953
Amount recalled
8,794

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

  • Nationwide
  • PR

Why it was recalled

Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this malfunction occurs, the pump will alarm and infusion stops.

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.

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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 7, 2016 · Data as of Sep 19, 6:01 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.