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CareFusion 303, Inc.

CareFusion 303, Inc. Recalls

All product recalls associated with CareFusion 303, Inc..

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Recall Summary

Total Recalls

96

Past Year

21

Class I (Serious)

0

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 61–80 of 96 recalls

CareFusion 303, Inc.: BD Pyxis MedStation ES (Med ES Main) REF: 323. Intended ...

Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.

FDAFeb 23, 2024Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES,...

Automated dispensing cabinets, running affected software, and Windows 10 operating system may experience the application randomly hang, freeze and/or crash, which may result in delays in medication access, and potential data loss.

FDAFeb 1, 2024Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLE...

If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first requiring the RxVerify Validation Code be entered/without validation from a pharmacist, which could lead to unintended and incorrect medication removal.

Page 4 of 5Next

Moderate

FDAOct 5, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: Alaris PCA Module 8120

Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

FDASep 15, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Alaris Syringe Module, REF 8110

Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

FDASep 15, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Alaris PCU REF 8015

Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

FDASep 15, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis CII Safe ES, REF: 1116-00; and BD Pyxis : CII Sa...

When global edit is used to update multiple formulary properties simultaneously, the following properties: 1) Require Lot Number on Recall, 2) Access Destruction Bin (Witness), 3) Add to Destruction Bin (Count/Empty), 4) CII Safe Stock Out Notice are, without user warning, overwritten to the value NO , which could result in diversion of controlled substances from the automated dispensing cabinet.

FDASep 6, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedBank MedPass Software, REF: 139088-01

After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.

FDAAug 18, 2023FL, KS, MI• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107...

Automated dispensing cabinet devices plugged into any multi-socket outlet power strips may present unacceptable levels of current leakage, which could expose users to system downtime and/or potential electric shock.

FDAMay 22, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD P...

Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.

FDAApr 5, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis Med ES Auxiliary (AUX), REF 343

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedStation ES AUX, REF 324

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedStation 4000 Main, REF 303

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis Med 4000 Auxiliary (AUX), REF 314

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedStation ES (Med ES Main), REF 323

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedS...

Due to an increase in complaints of door latch assembly failures that may cause the doors to be left in an open state potentially causing inventory discrepancies, a delay in access to medication and/or diversion of medication.

FDAFeb 14, 2023AL, AK, AZ +49 more• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxi...

Automated dispensing cabinet drawer firmware may have inadvertently been downgraded to an earlier version of drawer firmware during new device installations or device replacement upgrades, which may lead to an increased frequency of drawer failures, which could increase the likelihood of patients experiencing delays in receiving medications.

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedStation 4000 AUX, REF 306

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

FDAFeb 14, 2023Nationwide• CareFusion 303, Inc.

CareFusion 303, Inc.: Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g ...

Infusion pump PCs with specific software/network cards/IP addresses can have network/wireless connection failure. Could cause inability to receive new datasets and inability to transfer retrospective analytics data to connected systems. Users with interfaces to electronic medication record or admin discharge transfer, may be unable to receive/send data; infusions may need to be manually programmed

FDAJan 24, 2023AL, AK, AZ +47 more• CareFusion 303, Inc.

CareFusion 303, Inc.: BD Pyxis MedBank System - Product Label/labeling pending

Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.

FDADec 12, 2022Nationwide• CareFusion 303, Inc.