Reported Mar 5, 2025 · Ongoing

BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing…

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?

  • BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing Cabinet (ADC) intended to securely store and dispense medications and supplies to a qualified and authorized user in a clinical setting.
Lot codes and dates
  • BD Pyxis MedFlex 2.0
  • Catalog Number1139-00
  • UDI-DI code10885403512704
  • Serial/Lot Numbers

    229 of 229 codes

    • 16188677
    • 16234871
    • 16234918
    • 16234919
    • 16234920
    • 16235771
    • 16235773
    • 16235774
    • 16235776
    • 16235777
    • 16235778
    • 16235779
    • 16235780
    • 16237465
    • 16237466
    • 16237807
    • 16237809
    • 16237810
    • 16237811
    • 16237812
    • 16237813
    • 16238647
    • 16245711
    • 16245712
    • 16245713
    • 16245718
    • 16248197
    • 16248200
    • 16248203
    • 16248207
    • 16248208
    • 16248209
    • 16248211
    • 16248214
    • 16248216
    • 16248217
    • 16249389
    • 16249390
    • 16249392
    • 16249393
    • 16249394
    • 16249395
    • 16253258
    • 16253259
    • 16253260
    • 16253261
    • 16253264
    • 16253421
    • 16253423
    • 16255087
    • 16255088
    • 16255089
    • 16255090
    • 16255091
    • 16255092
    • 16255093
    • 16255094
    • 16255648
    • 16255649
    • 16255650
  • Bio-ID Spare Part Catalog Number353200-01
  • UDI-DI code10885403450136 No Serial/Lot Numbers provided since BD CareFusion is not the manufacturer of the spare parts
Amount recalled
229 MedFlex and 3,154 spare Bio-ID spare parts

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

Why it was recalled

Due to fingerprint scanner failing resulting in the scanner heating up.

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

Data as of Sep 19, 6:58 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.