PlainRecalls

CareFusion 303, Inc.

105 recalls on record · Latest: Jan 14, 2026

CareFusion 303, Inc. Recall Insight

CareFusion 303, Inc. appears on 105 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.125% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Jan 14, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 4 critical, 45 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 46 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Jun 5, 2024 to Jan 14, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Jan 14, 2026

BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03, 139676-01, 139421-01, 139420-…

FDA Devices Moderate Dec 31, 2025

BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro 7-…

FDA Devices Critical Nov 26, 2025

BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100, REF: 49000270. Used with …

FDA Devices Moderate Nov 5, 2025

BD Pyxis Pro MedStation Main, REF: 1155-00

FDA Devices Moderate Nov 5, 2025

Various models of BD Pyxis MedFlex, Reference numbers: 1119-00 1139-00 139038-01 139039-01 139040-01 139041-01 139043-01 139044-01 139045-01…

FDA Devices Moderate Nov 5, 2025

Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers: 1149-00 and 1152-00

FDA Devices Critical Oct 15, 2025

BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10…

FDA Devices Low Aug 20, 2025

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI 4HH/169-112, BD PYXIS MEDBANK …

FDA Devices Critical Aug 13, 2025

BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D DEHP FREE 3SS CV; REF: 2…

FDA Devices Moderate Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation 4000 Main 10885403512629 [303]…

FDA Devices Moderate Apr 23, 2025

MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK MINI MAIN, REF: 1147-00 BD PY…

FDA Devices Moderate Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated dispensing cabinets (ADC) intended …

FDA Devices Moderate Apr 16, 2025

BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 155141-01 BD PYXIS MEDBANK TWR MN CR-…

FDA Devices Moderate Mar 26, 2025

BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF: 1116-00, CII Safe ES Deskt…

FDA Devices Critical Mar 19, 2025

BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software

FDA Devices Moderate Mar 5, 2025

BD Alaris Pump Module REF 8100 The BD Alaris System with Guardrails Suite MX is a modular infusion pump and monitoring system for the continuous o…

FDA Devices Moderate Mar 5, 2025

138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 138911-01 BD PYXIS MEDBANK MINI CR-4HH-P 169-115 BD PYXIS MED…

FDA Devices Moderate Mar 5, 2025

139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS MEDFLEX MN 1000 12HH 139053-01 BD PYXIS MEDFLEX MN 1000 2HH-2FH-3FM 139041-01 BD PYXIS…

FDA Devices Moderate Feb 19, 2025

(1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES Tower, Catalog No. 352; (4)…

FDA Devices Moderate Feb 19, 2025

BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

FDA Devices Moderate Feb 5, 2025

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and Pyxis" MedStation 4000 ar…

FDA Devices Moderate Jan 29, 2025

BD Pyxis Med ES Auxiliary (AUX), REF 343

FDA Devices Moderate Jan 29, 2025

BD Pyxis MedStation 4000 Main, REF 303

FDA Devices Moderate Jan 29, 2025

BD Pyxis Med 4000 Auxiliary (AUX), REF 314

FDA Devices Moderate Jan 29, 2025

BD Pyxis MedStation ES (Med ES Main), REF 323

FDA Devices Moderate Jan 22, 2025

BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352

FDA Devices Moderate Dec 18, 2024

BD Pyxis CII Safe ES, REF: 1116-00

FDA Devices Moderate Dec 18, 2024

BD Pyxis MedStation ES 7 Drawer Auxiliary Tower, REF: 324

FDA Devices Moderate Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

FDA Devices Moderate Sep 25, 2024

Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system

FDA Devices Moderate Sep 25, 2024

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

FDA Devices Moderate Sep 25, 2024

Alaris PCA Module Model 8120, a modular infusion pump and monitoring system

FDA Devices Moderate Sep 25, 2024

Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring system

FDA Devices Moderate Sep 11, 2024

BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system

FDA Devices Moderate Aug 14, 2024

BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-2HH-6FH, REF: 169-88 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P, REF: 169-92 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-12HH-1FH, REF: 169-84 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9

FDA Devices Moderate Jul 24, 2024

BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES, REF: 1116-00; CII Safe ES,…

FDA Devices Moderate Jul 10, 2024

BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/ 169-101, MEDBANK MINI 1HH-1H…

FDA Devices Moderate Jul 10, 2024

BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 169-157, BD PYXIS MB TWR MN 1F…

FDA Devices Moderate Jul 10, 2024

BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units

FDA Devices Moderate Jun 5, 2024

BD Pyxis(TM) Anesthesia Station 4000, REF: 338

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds