Reported Sep 25, 2024 · Ongoing

Alaris Pump Module Model 8100, a modular infusion pump and monitoring system

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 Module Model 8100, a modular infusion pump and monitoring system
Lot codes and dates
  • Model Number8100
  • UDI-DI code
    • 10885403810046
    • 10885403810039
    • 10885403810015
  • Serial Numbers

    3,612 of 3,612 codes

    • 16448779
    • 16451711
    • 16451209
    • 16450973
    • 16450971
    • 16451760
    • 16407678
    • 16411676
    • 16388896
    • 16405467
    • 16408857
    • 16387206
    • 16405786
    • 16407463
    • 16410819
    • 16407769
    • 16399159
    • 16410420
    • 16411470
    • 16409931
    • 16409006
    • 16411571
    • 16409107
    • 16388799
    • 16472492
    • 16409660
    • 16410466
    • 16404846
    • 16409933
    • 16410968
    • 16406453
    • 16406013
    • 16408309
    • 16402653
    • 16410415
    • 16411500
    • 16411069
    • 16407539
    • 16410537
    • 16451801
    • 16450922
    • 16451705
    • 16448898
    • 16451601
    • 16448918
    • 16450847
    • 16453708
    • 16451857
    • 16451608
    • 16451642
    • 16372116
    • 16451808
    • 16451067
    • 16451690
    • 16451895
    • 16445957
    • 16453760
    • 16451083
    • 16453750
    • 16448376
Amount recalled
192964

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.

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 CareFusion 303, Inc. 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

Data as of Sep 19, 4:51 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.