Reported Mar 5, 2025 · Ongoing
BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis…
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 PyxisMedFlex
- REF1119-00
- MedBank Tower REF1145-00; MedBank MedPass
- REF139088-01 and associated BD Pyxis user/software/safety guides and quick reference guides
- Lot codes and dates
- User Guidesi. BD Pyxis MedBank Cabinet User Guide v2.4 ii. BD Pyxis MedBank MedPass User Guide v1.0 iii. BD Pyxis MedBank CR Station User Guide v3.10 iv. BD Pyxis MedBank myQLink Cloud Software User Guide v1.5 v. BD Pyxis Supply Cabinet Safety Guide (for SupplyBank
- models) Quick Reference Guidesi. BD Pyxis MedBank CR Station QRG (part number 155018-03) ii. BD Pyxis MedBank Cabinet QRG (PN 155023-03) iii. BD Pyxis MedBank RxNow CR Station QRG (PN 155026-03) iv. BD Pyxis MedBank RxNow Solution QRG 2.0 (PN 155027-02) v. BD Pyxis MedBank MedPass QRG (PN 155022-03) vi. BD Pyxis MedBank QFill Station QRG (PN 155020-02) vii. BD Pyxis MedBank myQLink Cloud Software QRG 3.0 (PN 155021-02)
- REF/UDI-DI/Serial Numbers
1,520 of 1,520 codes
1119-00/10885403512704/135170061352335013754724137679531378957513801727138261871387954413883357138848481393447213939327139487241403280214037891141581871415991614168580141728321417516214182716142023371422087214222746142281491422815014244101142548131425481614254812142548151427511214278095143179451431794614324386143320581434774714347748143491061434870814348709143524591436578614365785143749651437496314374964143770791437842814377908144075231440752414420205144202131442021114420207144202081442020614420223
- Amount recalled
- 1521
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
Automated dispensing device labeling is being updated to strengthen labeling around manual access to medications to address the risk of potential delays in retrieving contents/ accessing medications that may result from power loss or potential automated dispensing device malfunctions.
This product could cause temporary or reversible health problems — stop using it.
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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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