BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
type: Dataset
description: FDA recall Z-1928-2024 — CareFusion 303, Inc. is recalling BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.
license: https://creativecommons.org/publicdomain/zero/1.0/
is accessible for free: true
is part of: https://drug-device-safety-atlas.ryanjhunter.workers.dev/
is defined by: https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native
see also: https://agenticu.ryanjhunter.workers.dev/commons/the-research-object
date modified: 2026-06-24T07:02:03.626072+00:00
is based on: openFDA drug & device enforcement (recall) reports
  type: Dataset
  creator: U.S. Food & Drug Administration
about: BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
  type: MedicalDevice
  manufacturer: CareFusion 303, Inc.
claims: FDA recall Z-1928-2024: CareFusion 303, Inc. is recalling BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
claims: FDA classified recall Z-1928-2024 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-1928-2024
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-1928-2024
      status: recorded
  item list element: ListItem
    position: 2
    item:
      field: Product type
      value: Devices
      status: recorded
  item list element: ListItem
    position: 3
    item:
      field: Classification
      value: Class II
      status: determination
  item list element: ListItem
    position: 4
    item:
      field: Status
      value: Ongoing — the recall is still being carried out.
      status: recorded
  item list element: ListItem
    position: 5
    item:
      field: Recalling firm
      value: CareFusion 303, Inc.
      status: recorded
  item list element: ListItem
    position: 6
    item:
      field: Reason
      value: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
      status: recorded
  item list element: ListItem
    position: 7
    item:
      field: Initiated
      value: 2024-04-15
      status: recorded
  item list element: ListItem
    position: 8
    item:
      field: Lot/code info
      value: UDI: 10885403512629/Serial numbers added 8/27/2025: 13811918 13811919 8000118765 8000118766 12761424 12761425 12740622 12731265 12558708 15686451 15686452 15686453 15686454 15616386 15616388 15563539 15544140 15544141 15544142 15406815 15406817 15076403 15067076 15067081 15067083 15067085 15067088 15067091 15067095 15067096 15067098 15067099 15067100 15067103 15067104 15067108 15067109 15067110 15067111 15053373 15053374 15026036 15026038 14838460 14808782 14808783 14791224 14785171 14785172 14785173 14785174 14785175 14785176 14785177 14785178 14785179 14785180 14785181 14773852 14773853 14773855 14760077 14755527 14755528 14755529 14755530 14755531 14755532 14755533 14755534 14755535 14755536 14754778 14740957 14740958 14740959 14740960 14740961 14740962 14731697 14731699 14731700 14731701 14731702 14731703 14731704 14731705 14731706 14731707 14731708 14731709 14728147 14728148 14728149 14728150 14728151 14707852 14707853 14707854 14690161 14690162 14690163 14690165 14690167 14690168 14689034 14689041 14689042 14689043 14689044 14689045 14689046 14689047 14689048 14671931 14671932 14671933 14671934 14671935 14671936 14671937 14671938 14671939 14671943 14661055 14661056 14661057 14659557 14659558 14659559 14659560 14659561 14659562 14659565 14659566 14659567 14659568 14637284 14637285 14637292 14637293 14637295 14637297 14637298 14633424 14633425 14633426 14633427 14633428 14633429 14633437 14633439 14633440 14608821 14608822 14607298 14607300 14607301 14607302 14607303 14607304 14607305 14607315 14607317 14591184 14591187 14591188 14591189 14591190 14591191 14591192 14591193 14591194 14591195 14591196 14591197 14580305 14580307 14580310 14580314 14580315 14580316 14580317 14580318 14580319 14580320 14565979 14565980 14565998 14565999 14566000 14566001 14566002 14566003 14566004 14566005 14566006 14566007 14518498 14598304 14598305 14598306 14598307 14598308 13534422 14906228 14906230 14906232 14906234 14906236 14724815 14724816 14724817 14724818 14724819 14724820 …
      status: recorded
  item list element: ListItem
    position: 9
    item:
      field: Distribution pattern
      value: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of South Africa, Kuwait, Qatar, Singapore, Bermuda, United Arab Emirates, Argentina, Australia, Belgium, Bahrain, Brazil, Bahamas, Canada, Chile, China, Germany, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Italy, Japan, South Korea, Lebanon, Morocco, Mexico, New Zealand, Oman, Portugal, Thailand, Taiwan.
      status: recorded

FDA recall Z-1928-2024: CareFusion 303, Inc. is recalling BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet
type: Claim
text: The FDA logged enforcement record Z-1928-2024: CareFusion 303, Inc. is voluntarily recalling BD Pyxis MedStation 4000 System, REF: 303, Medication Cabinet — reason: Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.. Status: Ongoing — the recall is still being carried out.. Initiated 2024-04-15. Affected lots/codes: UDI: 10885403512629/Serial numbers added 8/27/2025: 13811918 13811919 8000118765 8000118766 12761424 12761425 12740622 12731265 12558708 15686451 15686452 15686453 15686454 15616386 15616388 15563539 15544140 15544141 15544142 15406815 15406817 15076403 15067076 15067081 15067083 15067085 15067088 15067091 15067095 15067096 15067098 15067099 15067100 15067103 15067104 15067108 15067109 15067110 15067111 15053373 15053374 15026036 15026038 14838460 14808782 14808783 14791224 14785171 14785172 14785173 14785174 14785175 14785176 14785177 14785178 14785179 14785180 14785181 14773852 14773853 14773855 14760077 14755527 14755528 14755529 14755530 14755531 14755532 14755533 14755534 14755535 14755536 14754778 14740957 14740958 14740959 14740960 14740961 14740962 14731697 14731699 14731700 14731701 14731702 14731703 14731704 14731705 14731706 14731707 14731708 14731709 14728147 14728148 14728149 14728150 14728151 14707852 14707853 14707854 14690161 14690162 14690163 14690165 14690167 14690168 14689034 14689041 14689042 14689043 14689044 14689045 14689046 14689047 14689048 14671931 14671932 14671933 14671934 14671935 14671936 14671937 14671938 14671939 14671943 14661055 14661056 14661057 14659557 14659558 14659559 14659560 14659561 14659562 14659565 14659566 14659567 14659568 14637284 14637285 14637292 14637293 14637295 14637297 14637298 14633424 14633425 14633426 14633427 14633428 14633429 14633437 14633439 14633440 14608821 14608822 14607298 14607300 14607301 14607302 14607303 14607304 14607305 14607315 14607317 14591184 14591187 14591188 14591189 14591190 14591191 14591192 14591193 14591194 14591195 …
claim type: official_fact
review status: current
commercial influence: false
epistemic status:
  occurred: true
  supported: true
  adjudged: true
  operative: true
grounding:
  grounding type: SourceCitation
  source: openFDA drug & device enforcement (recall) reports — U.S. FDA
  source url: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm
  value: Devices recall, status Ongoing
  adjudicator: openFDA drug & device enforcement (recall) reports — U.S. FDA
falsifier: A RECORD of measured/reported events (occurred=true) from openFDA drug & device enforcement (recall) reports — U.S. FDA; superseded when openFDA drug & device enforcement (recall) reports — U.S. FDA publishes its next release.

FDA classified recall Z-1928-2024 as Class II
type: Claim
text: The FDA assigned this recall Class II: Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.. This is the FDA's official risk classification — its regulatory DETERMINATION of the hazard category (a verdict constituted by the FDA's recognition, occurred=FALSE), adjudged=TRUE because the FDA issued it. It is NOT a measurement of harm to any specific person.
claim type: regulatory_determination
review status: current
commercial influence: false
epistemic status:
  occurred: false
  supported: true
  adjudged: true
  operative: true
grounding:
  grounding type: AdjudicativeAct
  source: U.S. FDA recall classification (openFDA enforcement)
  source url: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm
  value: Class II
  adjudicator: U.S. FDA recall classification (openFDA enforcement)
falsifier: occurred=FALSE: a regulatory DETERMINATION (an authority's classification/judgment) has NO material truthmaker independent of recognition — it is constituted by U.S. FDA recall classification (openFDA enforcement)'s say-so (a Searle institutional fact), not measured. adjudged=TRUE because U.S. FDA recall classification (openFDA enforcement) (an external authority) issued it. Distinct from a recorded measurement (which has an independent truthmaker) and from a modeled figure (a computed quantity, not a verdict). Challengeable; superseded if the authority reclassifies.

What an FDA recall is — and is NOT
type: Claim
text: A recall is a RECORDED FDA enforcement action — the FDA logged that a firm is removing or correcting a product, classed by the FDA's risk judgment. It does NOT establish that any specific unit is affected or caused harm; causation is not established. This record informs and compares — it is NOT medical advice and does not tell anyone to start or stop a drug or device. For a medical decision, route to the FDA recall record and a licensed pharmacist or prescriber.
claim type: interpretation
review status: current
commercial influence: false
epistemic status:
  occurred: false
  supported: true
  adjudged: false
  operative: true
grounding:
  grounding type: Interpretation
  source: Atlas Commons L5 boundary (enforcement-action ≠ harm causation)
  source url: https://drug-device-safety-atlas.ryanjhunter.workers.dev/
  value: a recorded enforcement action, not proof of harm or causation; not medical advice
falsifier: occurred=FALSE (a framing, not an event) and adjudged=FALSE (an in-house reading, not an authority's verdict) — the LOWEST-warrant claim here. A flat representation would render this identically to the official facts; the four-status does not.