BD Pyxis MedStation ES, REF: 323, Medication Cabinet
type: Dataset
description: FDA recall Z-1927-2024 — CareFusion 303, Inc. is recalling BD Pyxis MedStation ES, REF: 323, 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 ES, REF: 323, Medication Cabinet
  type: MedicalDevice
  manufacturer: CareFusion 303, Inc.
claims: FDA recall Z-1927-2024: CareFusion 303, Inc. is recalling BD Pyxis MedStation ES, REF: 323, Medication Cabinet
claims: FDA classified recall Z-1927-2024 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-1927-2024
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-1927-2024
      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: 10885403512667/New Serial Numbers reported 8/27/25: 14879021 15683381 15683382 15683385 15683386 15683387 15683388 15683389 15683390 15674988 15674992 15674993 15674994 15674995 15674996 15674998 15674999 15675000 15675001 15675036 15758077 15758078 15758079 15755497 15755499 15755501 15754424 17269762 13625680 13625681 13625682 13625684 13611196 13611198 13611204 13467008 13336011 13336013 13336014 13336015 13336016 14386862 14265629 14265630 14202688 14202689 14202690 14202691 14202692 14194839 14194841 14194842 14157202 14157203 14157204 14157205 14157206 14157207 14157208 14157209 14157210 14157211 14157212 13785825 13593077 13192143 13137112 13074966 13074968 13055699 13055700 13055726 13054792 13054060 13054061 13054101 12698939 17332556 17122344 16995995 16995997 16995998 16996016 16747803 16747804 16747805 16747843 16747844 16747988 15616385 15664565 15607464 15607465 15607466 15607495 15607497 15607498 15607499 15607501 15607503 15604320 15604321 15604323 15604324 15604326 15604327 15604328 15604329 15604330 15604331 15604332 15604333 15604334 15604336 15604363 15581091 17338599 17338602 16721620 16721621 16721623 16721625 16721627 15284381 15284382 15222320 15174016 15174029 15174030 14895248 14852791 14666440 14665877 14653429 14653430 14649023 14649024 14649026 14649027 14648431 14648432 14648433 14639938 14639940 14639160 14639162 14639315 14639316 14634709 14634710 14632403 14630545 14629441 14629442 14619333 14617921 14617922 14617923 14617926 14617927 14618342 14604018 14592478 14592479 14592480 14592481 14592482 14592483 14543160 14543161 14543162 14543163 14543164 14543166 14543167 14541637 14541639 14541658 14541661 14541663 14541664 14539223 14537571 14537572 14537573 14537574 14537578 14537579 14537580 14537583 14537589 14537590 14529072 14529073 14518470 14518471 14518475 14518480 14486061 14522390 14522391 14522392 14522393 14522397 14522398 14522399 14522401 14522402 14522403 14522405 14522406 14522407 14522409 14522410 14522416 14522417…
      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-1927-2024: CareFusion 303, Inc. is recalling BD Pyxis MedStation ES, REF: 323, Medication Cabinet
type: Claim
text: The FDA logged enforcement record Z-1927-2024: CareFusion 303, Inc. is voluntarily recalling BD Pyxis MedStation ES, REF: 323, 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: 10885403512667/New Serial Numbers reported 8/27/25: 14879021 15683381 15683382 15683385 15683386 15683387 15683388 15683389 15683390 15674988 15674992 15674993 15674994 15674995 15674996 15674998 15674999 15675000 15675001 15675036 15758077 15758078 15758079 15755497 15755499 15755501 15754424 17269762 13625680 13625681 13625682 13625684 13611196 13611198 13611204 13467008 13336011 13336013 13336014 13336015 13336016 14386862 14265629 14265630 14202688 14202689 14202690 14202691 14202692 14194839 14194841 14194842 14157202 14157203 14157204 14157205 14157206 14157207 14157208 14157209 14157210 14157211 14157212 13785825 13593077 13192143 13137112 13074966 13074968 13055699 13055700 13055726 13054792 13054060 13054061 13054101 12698939 17332556 17122344 16995995 16995997 16995998 16996016 16747803 16747804 16747805 16747843 16747844 16747988 15616385 15664565 15607464 15607465 15607466 15607495 15607497 15607498 15607499 15607501 15607503 15604320 15604321 15604323 15604324 15604326 15604327 15604328 15604329 15604330 15604331 15604332 15604333 15604334 15604336 15604363 15581091 17338599 17338602 16721620 16721621 16721623 16721625 16721627 15284381 15284382 15222320 15174016 15174029 15174030 14895248 14852791 14666440 14665877 14653429 14653430 14649023 14649024 14649026 14649027 14648431 14648432 14648433 14639938 14639940 14639160 14639162 14639315 14639316 14634709 14634710 14632403 14630545 14629441 14629442 14619333 14617921 14617922 14617923 14617926 14617927 14618342 14604018 14592478 14592479 14592480 14592481 14592482 14592483 14543160 14543161 14543162 14543163 14543164 14543166 14543167…
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-1927-2024 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.