BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324
type: Dataset
description: FDA recall Z-1929-2024 — CareFusion 303, Inc. is recalling BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324 (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 ES 7-Drawer Auxiliary Tower, REF: 324
  type: MedicalDevice
  manufacturer: CareFusion 303, Inc.
claims: FDA recall Z-1929-2024: CareFusion 303, Inc. is recalling BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324
claims: FDA classified recall Z-1929-2024 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-1929-2024
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-1929-2024
      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: 10885403512681/ Serial Numbers as of 8/27/2025:15674986 15674990 15674991 15674997 15758081 15758083 15755500 17280396 17275260 17275265 13611197 13611199 13611203 13467012 13336012 13336017 13336018 13336019 14386863 14265628 14194837 14157188 14157189 14157190 14157191 14157192 14157193 14157196 14157198 14157201 17578908 17578909 17338468 16726578 16726580 15222318 15222321 15284383 15222317 15167680 15167681 14823787 14648430 14648434 14648435 14639939 14639943 14639161 14639163 14639317 14634512 14634513 14634707 14634708 14634277 14630544 14629428 14539222 14537575 14537577 14537582 14537585 14537586 14537588 14518472 14522389 14522394 14522395 14522396 14522400 14522404 14522411 14522412 14522413 14522414 14522415 14522432 14522433 14522434 14522439 15686444 17437605 17437607 15576824 15558601 15554968 15554969 15548934 15597853 15597854 14677986 14672121 14672122 14672123 14671340 14671341 14671342 14671343 14666864 14666865 14666866 14666867 14663588 14657424 14655523 14649799 14649811 14649032 14619318 14619319 14619320 14617415 14617416 14617418 14617421 14617422 14617423 14617438 15454197 15064970 15064971 15064972 15064973 15064974 15064975 15064976 15064977 15064996 15064997 15064998 14890176 13822815 13796607 13796610 13796616 13796619 14016424 14016425 13651714 12786185 12786186 12772756 12772757 12741308 12741310 12741313 12741315 15561634 15561644 15561646 17338459 17338466 17338473 17338479 17338484 17338486 17338488 17338489 17338490 17338491 17338492 17338493 17338494 17338495 17338497 17338499 15561636 15561638 15496349 15496352 15496355 15496360 15496362 15496364 15496367 15496369 15496373 15496375 15496379 13736795 13736797 13736798 13055112 13055113 17338578 17338579 17338581 17338583 17222174 16951320 16951321 16951324 16951326 15742272 15742274 15720502 15105048 15105049 15066136 15066139 15000249 14952159 14801774 14801775 14801776 14801777 14801778 14801779 14801781 14801784 14470559 14439035 14119120 14119121 14119122 14081727 1403…
      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-1929-2024: CareFusion 303, Inc. is recalling BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324
type: Claim
text: The FDA logged enforcement record Z-1929-2024: CareFusion 303, Inc. is voluntarily recalling BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower, REF: 324 — 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: 10885403512681/ Serial Numbers as of 8/27/2025:15674986 15674990 15674991 15674997 15758081 15758083 15755500 17280396 17275260 17275265 13611197 13611199 13611203 13467012 13336012 13336017 13336018 13336019 14386863 14265628 14194837 14157188 14157189 14157190 14157191 14157192 14157193 14157196 14157198 14157201 17578908 17578909 17338468 16726578 16726580 15222318 15222321 15284383 15222317 15167680 15167681 14823787 14648430 14648434 14648435 14639939 14639943 14639161 14639163 14639317 14634512 14634513 14634707 14634708 14634277 14630544 14629428 14539222 14537575 14537577 14537582 14537585 14537586 14537588 14518472 14522389 14522394 14522395 14522396 14522400 14522404 14522411 14522412 14522413 14522414 14522415 14522432 14522433 14522434 14522439 15686444 17437605 17437607 15576824 15558601 15554968 15554969 15548934 15597853 15597854 14677986 14672121 14672122 14672123 14671340 14671341 14671342 14671343 14666864 14666865 14666866 14666867 14663588 14657424 14655523 14649799 14649811 14649032 14619318 14619319 14619320 14617415 14617416 14617418 14617421 14617422 14617423 14617438 15454197 15064970 15064971 15064972 15064973 15064974 15064975 15064976 15064977 15064996 15064997 15064998 14890176 13822815 13796607 13796610 13796616 13796619 14016424 14016425 13651714 12786185 12786186 12772756 12772757 12741308 12741310 12741313 12741315 15561634 15561644 15561646 17338459 17338466 17338473 17338479 17338484 17338486 17338488 17338489 17338490 17338491 17338492 17338493 17338494 17338495 17338497 17338499 15561636 15561638 15496349 15496352 15496355 15496360 15496362 15496364 1549636…
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-1929-2024 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.