Reported Aug 26, 2015 · Terminated

Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part…

CareFusion 303, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386

Is this the product you have?

  • Alaris Syringe Pump, Model No. 8110. Delivers fluids
  • Expansion of Affected UnitsBOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100
Lot codes and dates
  • 3,622 of 3,622 codes

    • 4051531
    • 4051532
    • 4051533
    • 4051534
    • 4051535
    • 4051684
    • 4051685
    • 4051686
    • 4051687
    • 4051688
    • 4051689
    • 4051690
    • 4051691
    • 4052487
    • 4052488
    • 4052489
    • 4052490
    • 4052492
    • 4052493
    • 4052495
    • 4052497
    • 4052499
    • 4052500
    • 4052501
    • 4052502
    • 4052503
    • 4052504
    • 4052505
    • 4052507
    • 4052509
    • 4052510
    • 4053437
    • 4053547
    • 4055907
    • 4059581
    • 4052494
    • 4052496
    • 4052508
    • 4052511
    • 4052491
    • 4052498
    • 4048982
    • 4048983
    • 4048985
    • 4048986
    • 4048987
    • 4048988
    • 4048990
    • 4048991
    • 4048992
    • 4048993
    • 4048994
    • 4048995
    • 4048996
    • 4048997
    • 4048999
    • 4049000
    • 4049002
    • 4049231
    • 4049232
    99
Amount recalled
68,460 units

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Channel Error code is displayed on the PC unit with an audio and visual alarm, and on the syringe module. After the error is cleared on the PCU, the syringe pump is unresponsive to key presses until the next power cycle, or the module is detached and reattached.

Using this product could cause serious injury, illness or death — stop using it now.

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 Dec 14, 2018 · Data as of Sep 19, 6:50 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.