CareFusion 303, Inc. recalls
Every recall we track for CareFusion 303, Inc. — 139 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 4 are rated “stop using now”.
Recalls per year, by danger level
Recalls from CareFusion 303, Inc. peaked in 2024 (44); 139 since 2017. 3% rated “stop using now”.
All FDA recall records for CareFusion 303, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 6 | 0 | 7 |
| 2018 | 0 | 2 | 0 | 0 | 2 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 1 | 15 | 9 | 0 | 25 |
| 2021 | 1 | 0 | 0 | 0 | 1 |
| 2022 | 0 | 1 | 1 | 0 | 2 |
| 2023 | 1 | 5 | 11 | 1 | 18 |
| 2024 | 0 | 7 | 37 | 0 | 44 |
| 2025 | 1 | 11 | 18 | 0 | 30 |
| 2026 (to date) | 0 | 4 | 5 | 0 | 9 |
Most common reasons for CareFusion 303, Inc. recalls
What to do if you have a recalled CareFusion 303, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All CareFusion 303, Inc. recalls
60 shown- Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
CareFusion recalls BD Pyxis MedBank Tower medication cabinets with serial numbers starting 10885403517167 due to fingerprint scanner overheating that may cause first-degree burns.
CareFusionApr 30, 2026 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
CareFusion 303, Inc. is a company that produces medical devices and equipment. They are known for their innovative solutions in the healthcare industry.
CareFusion 303, Inc.Feb 11, 2026 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,
Recall of BD Pyxis ES Enterprise Server devices with specific catalog numbers and software versions due to potential failure to receive timely patient and medication updates from enterprise systems.
BDDec 3, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower,
CareFusion recalls Pyxis MedStation ES models with firmware 1.48 due to potential access delays for medications. Affected units may need updates to prevent medication delays.
CareFusionNov 20, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a
Recall of BD Alaris Pump Module model 8100 with specific UDI-DI codes due to potential connectivity problems with hospital networks caused by daylight savings time adjustments.
BD AlarisNov 6, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100,
Recall of BD Alaris infusion pump modules 8100 and related parts due to risk of under/over-infusion if dropped or jarred. Affected units sold after June 19, 2004.
BD AlarisOct 17, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis Pro MedStation Main, REF: 1155-00
CareFusion recalls BD Pyxis Pro MedStation Main (REF 115:00) due to potential fluid ingress causing smoke, system downtime, or fire. Affected units have specific serial numbers.
CareFusionSep 30, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron
CareFusion recalls BD Alaris Pump Infusion Sets with specific reference numbers due to potential flow rate and bolus accuracy issues that could affect patient safety.
BD AlarisSep 11, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI
CareFusion 303, Inc. is a leading manufacturer of medical devices and healthcare products. Explore their product catalog for the latest innovations in medical technology.
CareFusion 303, Inc.Jul 10, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D
BD Alaris Pump Infusion Sets with specific model numbers may not deliver medication at correct flow rates or bolus doses, risking incorrect treatment. Affected units include those with back check valves and SmartSite Y-sites.
BD AlarisJul 8, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"
CareFusion recalls Pyxis medication dispensing systems due to antivirus software not being consistently installed during implementation, which could lead to security vulnerabilities.
CareFusionMay 8, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation
CareFusion recalls specific medical software systems that may delay medication access during cabinet upgrades due to software errors after Microsoft patches. Affected users should contact CareFusion for guidance.
CareFusionMay 8, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI
CareFusion recalls specific BD PYXIS MEDBANK models due to software error during pocket exchange restocking that could double medication counts and delay access to medicines.
BD PYXIS MEDBANKMar 11, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 155141-01 BD
BD Pyxis MedBank CUBIE Replenishment Stations with certain model numbers may show a stock error message when restocking, potentially delaying medication access for patients. Affected units include specific product codes listed in the recall.
BD PyxisMar 11, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated
BD Pyxis automated dispensing cabinets with software version 2.4 have a bug that can cause incorrect medication counts and extra doses. Affected units include MedBank Mini, Tower, MedFlex, and MedPass models.
BD PyxisMar 11, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
CareFusion recalls BD Alaris Systems Manager software versions 12.5.1 and 12.5.2 due to potential outdated automated programming requests for infusion units. Affected units may require updates to prevent safety issues.
BD AlarisFeb 18, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:
CareFusion recalls BD Pyxis Anesthesia Station ES models with specific software versions due to sync errors that could lead to incorrect medication dispensing. Affected units may need software updates to prevent safety issues.
CareFusionFeb 6, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis MedFlex 2.0 REF 1139-00 Bio-ID Spare Parts REF 353200-01 The BD Pyxis" MedFlex is an Automated Dispensing
Recalled BD Pyxis MedFlex 2.0 spare parts (REF 353200-01) have fingerprint scanners that heat up due to failure, potentially causing burns. Affected units include specific serial numbers listed in the recall.
BD CareFusionJan 23, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Alaris Pump Module REF 8100 The BD Alaris System with Guardrails Suite MX is a modular infusion pump and monitoring
CareFusion recalls BD Alaris Pump Module REF 8100 due to user manual error that may cause accidental overinfusion if safety clamp is left open. Affected units include those with software version 12.1.2.
CareFusionJan 23, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis
BD Pyxis MedFlex, MedBank Tower, and MedBank MedPass devices with specific reference numbers may have labeling updates to address potential delays in accessing medications during power loss or malfunctions. Users should review the updated guides and quick reference materials.
BD PyxisJan 10, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls (1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis
CareFusion recalls BD Pyxis MedStation and Anesthesia Station models with insufficient labeling for medication access delays. Users should check serial numbers and software versions to determine if affected.
BD PyxisJan 8, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls 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
CareFusion recalls BD PYXIS MEDBANK MINI models with labeling update to include contraindication against use in procedures and operating rooms.
CareFusionJan 8, 2025 - Lower riskMedical device
CareFusion 303, Inc. recalls (1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES
CareFusion recalls Pyxis MedStation ES and Anesthesia Station models with software issues that could cause wrong therapy doses, delays in dispensing, or unauthorized access. Affected units have specific catalog numbers and software versions.
CareFusionJan 8, 2025 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis CII Safe ES, REF: 1116-00
Recall of BD Pyxis CII Safe ES devices with software version 1116-00 due to risk of dispensing incorrect medications, potentially causing medication errors or stockouts. Affected units include specific serial numbers.
BD PyxisNov 14, 2024 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
CareFusion recalls Alaris EtCO2 Module Model 8300 infusion pumps due to potential bent connectors that could delay infusion starts. Affected units have specific serial numbers and UDI-DI codes.
CareFusionAug 15, 2024 - Use cautionMedical device
CareFusion 303, Inc. recalls BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system
CareFusion recalls Pyxis QFill Replenishment Station with potential for incorrect medication labels when restocking non-CUBIE locations. Affected units have specific serial numbers; contact CareFusion for remedy.
CareFusionJul 9, 2024 - Lower riskMedical device
CareFusion 303, Inc. recalls BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9
CareFusion recalls BD PYXIS medication dispensing cabinets with software version 3.9.1.9 due to potential incorrect bin labeling for medications. Affected units may print wrong storage locations for medications in automated dispensing cabinets.
BD PYXISJun 24, 2024 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units
CareFusion recalls BD Alaris System Manager REF 9601 software versions 12.5.1 due to wireless data transmission issues with compatible BD Alaris PC Units.
CareFusionMay 21, 2024 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/
Recalled BD Pyxis MedBank Mini devices with un-certified power strips may cause shocks or injury. Affected units sold Nov 2012-July 2023; check model numbers listed.
BD PyxisMay 13, 2024 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES,
BD Pyxis MedStation ES devices with specific software versions may prevent medication access if Component Manager is configured to 'installed mode' and software patch KB 5033688 is installed. Affected units include MedStation ES (Main), Tower, Anesthesia Station ES, and CII Safe ES models.
BD PyxisMay 2, 2024 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis(TM) Anesthesia Station 4000, REF: 338
CareFusion 303, Inc. is a leading manufacturer of medical devices and healthcare products. Explore their product catalog for detailed information on their latest innovations.
CareFusion 303, Inc.Apr 15, 2024 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized
CareFusion recalls BD Pyxis MedStation 4000 medication cabinets due to potential drawer and door failures that could delay medication access. Affected units have specific serial numbers.
CareFusionFeb 23, 2024 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower, REF: 352;
BD Pyxis MedStation ES models with software versions 1.4.x, 1.5.x, or 1.6.x may freeze, causing medication delays and data loss. Affected units include MedStation ES (REF 323), Anesthesia Station ES (REF 327), and MedStation ES Tower (REF 352).
BD PyxisFeb 1, 2024 - Use cautionMedical device
CareFusion 303, Inc. recalls MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK
CareFusion recalls MEDFLEX and MEDBANK automated dispensing cabinets that could dispense medication without pharmacist validation if 'Clear All' is selected on patient profiles.
CareFusionOct 5, 2023 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris PCA Module 8120
CareFusion recalls Alaris PCA Module 8120 infusion pumps with unvalidated syringe labeling. This could lead to incorrect medication delivery. Affected units have specific serial numbers.
CareFusionSep 15, 2023 - UnratedMedical device
CareFusion 303, Inc. recalls BD Pyxis CII Safe ES, REF: 1116-00; and BD Pyxis : CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01; CII Safe ES
BD Pyxis CII Safe ES software versions 1.7.3 and 1.7.4 may overwrite controlled substance properties without warning, risking diversion of controlled substances. Affected units include specific model numbers and software versions.
BD PyxisSep 6, 2023 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis MedBank MedPass Software, REF: 139088-01
BD recalls software versions before v1.2.3.23 for duplicate medication dispensing risks. Affected users should update to fix the issue.
BDAug 18, 2023 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,
Recall of BD Pyxis CII Safe software versions V7-V9 with specific model numbers due to potential electric shock from power strips. Affected devices may need repair or replacement.
BD Pyxis CII SafeMay 22, 2023 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES (Med ES Main Tower), REF: 352; BD Pyxis
CareFusion recalls Pyxis MedStation ES devices with software versions 1.7.0-1.7.4 due to potential patient data loss and medication errors. Affected units may show incorrect medication information.
CareFusionApr 5, 2023 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352
CareFusion recalls BD Pyxis MedStation ES models with software v1.7.3 due to potential delayed therapy when multi-component orders fail to display available items. Affected units may need software update.
CareFusionApr 5, 2023 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation
CareFusion recalls Pyxis Anesthesia ES and MedStation systems with outdated drawer firmware that may cause medication delays for patients. Affected units have specific model numbers and serial codes.
CareFusionFeb 14, 2023 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and
CareFusion 303
CareFusion 303Feb 14, 2023 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis Med ES Auxiliary (AUX), REF 343
CareFusion 303, Inc. is a manufacturer of medical devices and products. This page lists all their products.
CareFusion 303, Inc.Feb 14, 2023 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to
CareFusion recalls Alaris PC Units 8015 with specific software and wireless network cards that may fail to connect, risking infusion data transfer issues. Affected units have IP addresses from x.x.x.224 to x.x.x.255.
CareFusionJan 24, 2023 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Pyxis MedBank System - Product Label/labeling pending
CareFusion 303, Inc. is a company that produces medical devices and products. This page lists their product catalog.
CareFusion 303, Inc.Dec 12, 2022 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex
Recall of BD Pyxis MedBank Cabinets with Matrix Drawers using software v2.1.2.9. Update causes cabinet to stop functioning, delaying medication access in healthcare facilities.
BD PyxisMay 24, 2022 - Stop using nowMedical device
CareFusion 303, Inc. recalls BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad; and Pump Module Door Assembly Replacement Kit with Pump
BD Alaris recalls infusion pump modules with faulty keypads that may cause unresponsive keys, leading to medication infusion errors. Affected units were manufactured from January 2019 to December 2019. Contact for replacement.
BD AlarisMar 3, 2021 - Stop using nowMedical device
CareFusion 303, Inc. recalls BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon
BD Alaris EtCO2 module recall for potential monitoring interruption in patient care. Affected units include specific model and serial numbers. Stop using immediately to prevent patient safety risks.
BD AlarisAug 4, 2020 - Lower riskMedical device
CareFusion 303, Inc. recalls BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;
CareFusion recalls BD Alaris System devices with model numbers 8110 and 8120 that may display incorrect syringe types or sizes, potentially causing infusion delays, under-infusion, or over-infusion. Affected units include specific serial numbers listed in the recall.
CareFusionAug 4, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris System PC Unit Model 8015
CareFusion recalls Alaris System PC Unit Model 8015 (serials from April 7, 2017) due to unresponsive keypad keys that may cause infusion delays or interruptions, risking serious injury or death for high-risk patients.
CareFusionAug 4, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls BD Alaris System PC Unit Model 8100 (Pump Module) and Pump Module Door Assembly Replacement Kits (P/N 49000239,
BD Alaris System PC Unit Model 8100 pump modules may have unresponsive keys due to fluid ingress, risking infusion delays that could cause serious injury or death in high-risk patients.
BD AlarisAug 4, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris Pump Module Model 8100
CareFusion recalls Alaris Pump Module Model 8100 with all serial numbers due to broken elements that may cause inaccurate fluid delivery, over or under infusion risks.
CareFusionJun 30, 2020 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to
CareFusion recalls Alaris Syringe Module Model 8110 for potential dim LED display that could lead to inaccurate infusion monitoring. Affected units have specific serial numbers.
CareFusionJun 30, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris System PC Unit Model 8015. modular infusion pump and monitoring system
CareFusion recalls Alaris System PC Unit Model 8015 due to loose screws causing battery power loss and potential interruption of patient therapy. All units with serial numbers are affected.
CareFusionJun 30, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris System PC Unit Model 8015, a modular infusion pump and monitoring system
CareFusion recalls Alaris System PC Unit Model 8015 due to cleaning agents potentially damaging connectors, causing infusion interruptions. Affected units require specific cleaning steps to prevent therapy interruptions.
CareFusionJun 30, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)
CareFusion recalls Alaris PC units 8000 (v9.5 or older) and 8015 (v12.1.0 or 9.33 or older) due to software errors that could interrupt insulin therapy. Affected users should check their device version and contact CareFusion for updates.
CareFusionFeb 4, 2020 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933
CareFusion recalls Alaris EtCO2 Model 8300 devices with specific serial numbers due to potential calibration errors using lower CO2 concentrations during manufacturing, which may cause inaccurate blood gas readings.
CareFusionJul 1, 2019 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris Pump Module/Medley Pump Module/Gemini
CareFusion recalls Alaris infusion pump sets that users cannot prime. These sets may cause fluid flow issues. Stop using immediately to prevent potential complications.
CareFusionApr 20, 2018 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following
CareFusion recalls Alaris Pump Model 8100 units with FR-110 plastic bezels made between April 2011 and June 2017 due to potential weakening that could cause infusion errors.
CareFusionApr 13, 2018 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA
CareFusion recalls Alaris PCA Pump Model 8120 due to risk of syringe plunger grippers failing to close properly, potentially causing medication delivery issues.
CareFusionNov 17, 2017
CareFusion 303, Inc. recall questions
How many recalls has CareFusion 303, Inc. had?
139 recalls from CareFusion 303, Inc. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent CareFusion 303, Inc. recall?
CareFusion 303, Inc. recalls BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet, dated Apr 30, 2026. Every CareFusion 303, Inc. recall is listed on this page, newest first.
Why are CareFusion 303, Inc. products recalled?
The most common reasons on record: Fingerprint scanner may overheat to a temperature to cause 1st degree burn. (8).
What should I do if I have a recalled CareFusion 303, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new CareFusion 303, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.