Reported Dec 30, 2015 · Terminated

Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or…

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

Is this the product you have?

  • Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or vein.
Lot codes and dates
  • 68 of 68 codes

    • 15086733
    • 15086937
    • 15095168
    • 15095332
    • 15095772
    • 15096137
    • 15096516
    • 15086756
    • 15095022
    • 15095212
    • 15095333
    • 15095773
    • 15096183
    • 15096627
    • 15086832
    • 15095045
    • 15095213
    • 15095334
    • 15095842
    • 15096184
    • 15096628
    • 15086833
    • 15095088
    • 15095214
    • 15095347
    • 15095843
    • 15096222
    • 15096629
    • 15086864
    • 15095103
    • 15095254
    • 15095490
    • 15095844
    • 15096291
    • 15096703
    • 15086865
    • 15095128
    • 15095255
    • 15095504
    • 15095936
    • 15096292
    • 15096704
    • 15086910
    • 15095136
    • 15095274
    • 15095505
    • 15096020
    • 15096412
    • 15096722
    • 15086911
    • 15095137
    • 15095275
    • 15095561
    • 15096021
    • 15096413
    • 15096723
    • 15086912
    • 15095166
    • 15095289
    • 15095644
Amount recalled
1,445,180 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

  • Nationwide

Why it was recalled

CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set because the disconnection and leakage may occur during infusion.

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 Mar 1, 2017 · 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.