BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
type: Dataset
description: FDA recall Z-1930-2024 — CareFusion 303, Inc. is recalling BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306 (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 7-Drawer Auxiliary Tower, REF: 306
  type: MedicalDevice
  manufacturer: CareFusion 303, Inc.
claims: FDA recall Z-1930-2024: CareFusion 303, Inc. is recalling BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
claims: FDA classified recall Z-1930-2024 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-1930-2024
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-1930-2024
      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: 10885403512636/Serial Numbers added 8/27/2025: 12558525 13351845 15616389 15616390 15616391 15563540 15544135 15544136 15544137 15544138 15544139 15406818 15358663 15067079 15067087 15067090 15067097 15067101 15067102 15067106 15067107 14785182 14785183 14785184 14785185 14689030 14689031 14689033 14671361 14671362 14671363 14671364 14671365 14671366 14671367 14671369 14671370 14659569 14659570 14659571 14659572 14659573 14659574 14659576 14659577 14659578 14639957 14637299 14637300 14637301 14637302 14637303 14637304 14633430 14633431 14633432 14633433 14633434 14633435 14633436 14607306 14607307 14607308 14607309 14607310 14607311 14607312 14607313 14607314 14590696 14590697 14590698 14590699 14590700 14590702 14590703 14578551 14578552 14578553 14578554 14578555 14578556 14578558 14578559 14565988 14565989 14565990 14565991 14565992 14565993 14565994 14565995 14565996 14565997 14598309 15777264 15570731 15110842 14906229 14906231 14906233 14906235 14906237 14906238 14724865 14724866 14724867 14724868 14724869 14724870 14724871 14724872 14724873 14724875 14724876 14724877 14724878 14147868 14895210 14895212 8000132477 8000132478 12458388 12453585 14771237 14771238 13419887 13419888 14054009 13720803 13720812 13720815 13720817 13720829 13720832 13720836 13720839 13720841 13720843 13720847 13720850 13720854 13720863 13720866 13720871 13720878 13720880 13720882 13720884 13720888 13720893 13720894 13720899 13720902 13720908 13668699 13668700 13668701 13662199 13647263 13647264 13838583 8000090022 8000090023 8000091120 8000091121 8000091122 8000091124 8000091125 8000091126 8000094985 8000094987 8000094988 12794937 8000054590 13218022 13024432 13840570 13839433 15107217 15107218 15107219 15024443 13701499 15770171 15107202 15107203 15107204 15107206 15107207 15107208 15107209 15107210 15107211 15107212 15107216 15107221 15107222 15107223 15107224 15107225 15107226 15107227 15024445 15024446 15024447 15024448 15024449 14629650 12719020 14373401 8000037077 8000063807…
      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-1930-2024: CareFusion 303, Inc. is recalling BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306
type: Claim
text: The FDA logged enforcement record Z-1930-2024: CareFusion 303, Inc. is voluntarily recalling BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower, REF: 306 — 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: 10885403512636/Serial Numbers added 8/27/2025: 12558525 13351845 15616389 15616390 15616391 15563540 15544135 15544136 15544137 15544138 15544139 15406818 15358663 15067079 15067087 15067090 15067097 15067101 15067102 15067106 15067107 14785182 14785183 14785184 14785185 14689030 14689031 14689033 14671361 14671362 14671363 14671364 14671365 14671366 14671367 14671369 14671370 14659569 14659570 14659571 14659572 14659573 14659574 14659576 14659577 14659578 14639957 14637299 14637300 14637301 14637302 14637303 14637304 14633430 14633431 14633432 14633433 14633434 14633435 14633436 14607306 14607307 14607308 14607309 14607310 14607311 14607312 14607313 14607314 14590696 14590697 14590698 14590699 14590700 14590702 14590703 14578551 14578552 14578553 14578554 14578555 14578556 14578558 14578559 14565988 14565989 14565990 14565991 14565992 14565993 14565994 14565995 14565996 14565997 14598309 15777264 15570731 15110842 14906229 14906231 14906233 14906235 14906237 14906238 14724865 14724866 14724867 14724868 14724869 14724870 14724871 14724872 14724873 14724875 14724876 14724877 14724878 14147868 14895210 14895212 8000132477 8000132478 12458388 12453585 14771237 14771238 13419887 13419888 14054009 13720803 13720812 13720815 13720817 13720829 13720832 13720836 13720839 13720841 13720843 13720847 13720850 13720854 13720863 13720866 13720871 13720878 13720880 13720882 13720884 13720888 13720893 13720894 13720899 13720902 13720908 13668699 13668700 13668701 13662199 13647263 13647264 13838583 8000090022 8000090023 8000091120 8000091121 8000091122 8000091124 8000091125 8000091126 8000094985 8000094987 …
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-1930-2024 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.