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Use caution Medical device recall · FDA · Published May 22, 2023

BD Pyxis CII Safe Software V7-V9 Recalls: Electric Shock Risk from Power Strips

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2094-2023Medical deviceBD Pyxis CII Safe ›
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Contact the company

Recalling firmCareFusion 303, Inc.10020 Pacific Mesa Blvd · San Diego, CA 92121-4386
✎ GovInfoNow plain-language explainer

CareFusion recalls BD Pyxis CII Safe software versions V7 through V9 that were sold with certain model numbers. These devices could cause electric shock if plugged into multi-socket power strips due to current leakage. Read more at govinfonow.com/recall/58135-bd-pyxis-cii-safe-software-v7-v9-recalls-electric-shock.

Source Summary by GovInfoNow · govinfonow.com/recall/58135-bd-pyxis-cii-safe-software-v7-v9-recalls-electric-shock · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2094-2023

Cite this page

“BD Pyxis CII Safe Software V7-V9 Recalls: Electric Shock Risk from Power Strips.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58135-bd-pyxis-cii-safe-software-v7-v9-recalls-electric-shock. Based on FDA recall #Z-2094-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2094-2023%22&limit=1).

The FDA announced on May 22, 2023, that CareFusion 303, Inc. is recalling BD Pyxis CII Safe automated dispensing cabinet devices due to unacceptable current leakage levels when plugged into multi-socket outlet power strips. The hazard poses a risk of system downtime and potential electric shock to users.

How to tell if you have it

  • BD Pyxis CII Safe, Software: V7, REF: 107-96
  • BD Pyxis CII Safe, Software: V7, REF: 107-97
  • BD Pyxis CII Safe, Software: V7, REF: 107-97-201
  • BD Pyxis CII Safe, Software: V7, REF: 107-223
  • BD Pyxis CII Safe, Software: V8, REF: 111-199-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-200-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-201-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-202-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-203-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-204-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-205-01
  • BD Pyxis CII Safe, Software: V8, REF: 111-206-01
  • BD Pyxis CII Safe, Software: V8, REF: 107-245-01
  • BD Pyxis CII Safe, Software: V8, REF: 107-246-01
  • BD Pyxis CII Safe, Software: V9, REF: 107-252-01
  • BD Pyxis CII Safe, Software: V9, REF: 111-215
  • BD Pyxis CII Safe, Software: V9, REF: 111-216
  • BD Pyxis CII Safe, Software: V9, REF: 111-219
  • BD Pyxis CII Safe, Software: V9, REF: 111-221
  • BD Pyxis CII Safe, Software: ES, REF: 107-254-01
  • BD Pyxis CII Safe, Software: ES, REF: 107-255-01
  • BD Pyxis CII Safe, Software: ES, REF: 1116-00
  • BD Pyxis CII Safe, Software: ES, REF: 1117-00
  • BD Pyxis CII Safe, Software: N/A, REF: 111-113
  • BD Pyxis CII Safe, Software: N/A, REF: 111-114
  • BD Pyxis CII Safe, Software: N/A, REF: 111-115
  • BD Pyxis CII Safe, Software: N/A, REF: 111-160-201
  • BD Pyxis CII Safe, Software: N/A, REF: 111-217
  • BD Pyxis CII Safe, Software: N/A, REF: 111-218
  • BD Pyxis CII Safe, Software: N/A, REF: 111-220
  • BD Pyxis CII Safe, Software: N/A, REF: 111-222
  • Tripp Lite SUPER6TEL Surge Suppressor, REF: CN 200-025

The hazard

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

Context

GovInfoNow's records show CareFusion 303, Inc. has 64 other recalls on record since 2017-06-12. Other recent recalls of similar products include BD Pyxis MedStation ES Tower 352 Medication Cabinet Recall (2026-04-30), CareFusion - CareFusion labeling recall (2026-02-11), and BD Pyxis ES Enterprise Server Software Update Issue Recall (2025-12-03). Other recent recalls of similar products include Philips Allura Xper FD10C Medical System Recall (2025-12-15), Philips Allura Xper FD10F Medical System Recall (2025-12-15), and Spacelabs Ultraview SL Command Module Software Recall (2026-03-26).

How to tell if you have this one

Check if your BD Pyxis CII Safe system has software versions V7 through V9 with model numbers listed in the recall (e.g., 107-96, 107-97, 107-223, etc.). Devices manufactured from May 4, 2006, to September 26, 2023, are affected.

  • Brand
    BD Pyxis CII Safe
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Device Model

    Identify your BD Pyxis CII Safe model number and software version to see if it matches the recalled list (e.g., 107-96, 107-97, 107-223).

  2. Stop Using If Plugged into Power Strips

    If your device is plugged into a multi-socket power strip, disconnect it immediately to prevent electric shock.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 50 states.

Alaska: named in the noticeAKMaine: named in the noticeMEVermont: named in the noticeVTNew Hampshire: named in the noticeNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: named in the noticeMTNorth Dakota: named in the noticeNDMinnesota: named in the noticeMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: named in the noticeRIMassachusetts: named in the noticeMAOregon: named in the noticeORNevada: named in the noticeNVWyoming: named in the noticeWYSouth Dakota: named in the noticeSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: named in the noticeCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: named in the noticeCONebraska: named in the noticeNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: named in the noticeWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: named in the noticeNMKansas: named in the noticeKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: named in the noticeDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: named in the noticeHITexas: named in the noticeTXFlorida: named in the noticeFLPuerto Rico: named in the noticePR

FDA distribution: “US Nationwide-Worldwide Distribution: CO, MS, HI, FL, GA, CA, ND, GU, DE, MO, DC, SC, VA, AK, TX, NY, MN, PA, MA, OH, WI, NC, KY, KS, IL, MD, NE, MI, IA, WA, NM, LA, OK, AZ, AR, IN, WY, AL, NJ, SD, NV, TN, OR, WV, ME, ID, CT, UT, RI, MT,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 51 days after the firm started it.

1. Firm started the recall: May 22, 202312. FDA classified it Class II: Jul 5, 202323. Published in FDA’s Enforcement Report: Jul 12, 202332023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-2094-2023 (May 22, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2094-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA