Recalled BD Pyxis automated dispensing cabinets with unverified power strips that may cause electrical shock. Affected models include BD PYXIS MB TOWER MAIN variants from Nov 2012 to July 2023. Contact manufacturer for details.
Multiple socket-outlet power strips that shipped with automated dispensing cabinet devices have not been certified to International Electrotechnical Commission (IEC) electrical standards when used as a system with automated dispensing cabinet devices, so use may expose user to leakage currents that could cause varying degrees of harm from a minor shock to permanent impairment.
CareFusion 303, Inc. is recalling certain BD Pyxis automated dispensing cabinets because the power strips included may not meet electrical safety standards. Using these cabinets could expose users to electrical shocks ranging from minor shocks to serious injury.
The power strips that came with these cabinets were not certified to international electrical safety standards. When used with the cabinets, they can cause leakage currents that may result in electrical shocks, from minor shocks to serious injury or permanent harm.
Healthcare facilities and medical professionals who use BD Pyxis automated dispensing cabinets with the listed models. Patients and staff are at risk if the cabinets are used without proper electrical safety.
Check for model numbers like BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, or BD PYXIS MB TOWER MAIN W/MP/ on the cabinet. These models were manufactured from November 15, 2012, to July 25, 2023.
Inspect the power strips included with the cabinet for the model numbers listed in the recall notice.
Reach out to CareFusion 303, Inc. for specific guidance on the affected models and next steps.
The affected models include BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/, and other variants listed in the recall notice.
These cabinets were manufactured from November 15, 2012, to July 25, 2023.
The recall notice does not specify a fix; users are advised to contact CareFusion 303, Inc. for details on affected models and next steps.
We’ve drafted a message you can send BD Pyxis to request your refund or repair — edit it as you like.
Subject: Recall Z-2256-2024 — BD Pyxis BD Pyxis Hello, I own a BD Pyxis that is covered by recall Z-2256-2024 from BD Pyxis. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
