CareFusion 303 recalls

CareFusion 303 has 143 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 10 Jun 2026. 98 are still ongoing. 18 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls143since 2012

Last 12 months18reported

Class I3424% of total

Ongoing98latest 10 Jun 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 1 4 5Feb 10 4 0May 0 1 3Aug 0 1 6Nov 1 1 1Feb 0 0 0May 8 0 0Aug 0 0

Severity split

Class I 34 24%Class II 108 76%Class III 1 1%

Why carefusion 303 is recalled

Product types

By year

2026107%
20253524%
20242820%
2023107%
202211%
202111%
20202316%
201921%
201832%
201786%

Ongoing carefusion 303 recalls

98 active

Reported	Class	Recall	Company	Reason	Where
10 Jun 2026Device	CLASS II	BD Pyxis MedStation ES Tower recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedBank Mini recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedStation recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis Anesthesia Station ES recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedStation ES recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis Anesthesia Station recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide

All carefusion 303 recalls, newest first

143 total

Reported	Class	Recall	Company	Reason	Where
10 Jun 2026Device	CLASS II	BD Pyxis MedStation ES Tower recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedBank Mini recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedStation recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis Anesthesia Station ES recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedStation ES recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis Anesthesia Station recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis Mini Main recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
10 Jun 2026Device	CLASS II	BD Pyxis MedBank Tower recalled by CareFusion 303	CareFusion 303	Temperature Abuse	Nationwide
4 Feb 2026Device	CLASS II	BD Alaris" Pump Module recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
14 Jan 2026Device	CLASS II	BD Pyxis ES Enterprise Server recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
31 Dec 2025Device	CLASS II	BD Pyxis MedStation ES recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
26 Nov 2025Device	CLASS I	BD Alaris infusion Pump Module recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
5 Nov 2025Device	CLASS II	Various models of BD Pyxis Medbank: Reference numbers recalled	CareFusion 303	Other	Nationwide
5 Nov 2025Device	CLASS II	All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF recalled	CareFusion 303	Other	Nationwide
5 Nov 2025Device	CLASS II	Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers recalled	CareFusion 303	Other	Nationwide
5 Nov 2025Device	CLASS II	Various models of BD Pyxis MedFlex, Reference numbers recalled	CareFusion 303	Other	Nationwide
5 Nov 2025Device	CLASS II	BD Pyxis Pro MedStation Main recalled by CareFusion 303	CareFusion 303	Other	Nationwide
15 Oct 2025Device	CLASS I	BD Alaris Pump Infusion Sets recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
20 Aug 2025Device	CLASS III	Description/REF: BD Pyxis Medbank Mini 1FH-1FM/169-137, BD Pyxis recalled	CareFusion 303	Other	Nationwide
13 Aug 2025Device	CLASS I	BD Alaris Pump Module recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
13 Aug 2025Device	CLASS I	BD Alaris Pump Infusion Sets recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
2 Jul 2025Device	CLASS II	Product Name [ recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
30 Apr 2025Device	CLASS II	BD Pyxis Medbank (Name recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
23 Apr 2025Device	CLASS II	Medflex, REF: 1119-00; Medbank Main, REF: 1137-00; Medflex 2.0, REF recalled	CareFusion 303	Device Malfunction	Nationwide
16 Apr 2025Device	CLASS II	BD Pyxis MedBank Cubie Replenishment Station Product recalled	CareFusion 303	Device Malfunction	32 states
16 Apr 2025Device	CLASS II	BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower recalled	CareFusion 303	Device Malfunction	Nationwide
26 Mar 2025Device	CLASS II	BD Pyxis: Anesthesia Station ES recalled by CareFusion 303	CareFusion 303	Device Malfunction	Nationwide
19 Mar 2025Device	CLASS I	BD Care Coordination Engine (CCE) Infusion Adapter recalled	CareFusion 303	Device Malfunction	21 states
19 Mar 2025Device	CLASS I	BD Alaris Systems Manager recalled by CareFusion 303	CareFusion 303	Device Malfunction	21 states
5 Mar 2025Device	CLASS II	BD Pyxis MedFlex recalled by CareFusion 303	CareFusion 303	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.