Z-0453-2026.jsonld
type: Dataset
name: Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE MONITOR B450 (ATO MODEL) 2068491-002 CARESCAPE MONITOR B450 B1 2107633-001 CARESCAPE MONITOR B450-GS (V2.0.8) 2094080-001
description: FDA recall Z-0453-2026 — GE Healthcare Finland Oy is recalling Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE MONITOR B450 (ATO MODEL) 2068491-002 CARESCAPE MONITOR B450 B1 2107633-001 CARESCAPE MONITOR B450-GS (V2.0.8) 2094080-001 (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: MedicalDevice
  name: Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE MONITOR B450 (ATO MODEL) 2068491-002 CARESCAPE MONITOR B450 B1 2107633-001 CARESCAPE MONITOR B450-GS (V2.0.8) 2094080-001
  manufacturer: GE Healthcare Finland Oy
claims: enforcement-record
claims: FDA classified recall Z-0453-2026 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-0453-2026
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-0453-2026
      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: GE Healthcare Finland Oy
      status: recorded
  item list element: ListItem
    position: 6
    item:
      field: Reason
      value: Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
      status: recorded
  item list element: ListItem
    position: 7
    item:
      field: Initiated
      value: 2025-09-26
      status: recorded
  item list element: ListItem
    position: 8
    item:
      field: Lot/code info
      value: UDI-DI 00840682146135 Serial numbers SNT25079613SA SNT25079608SA SNT25079622SA SNT25079618SA SNT25079619SA SNT25079614SA SNT25079611SA SNT25079621SA SNT25079620SA SNT25079603SA SNT25079616SA SNT25079612SA SNT25079602SA SNT25079615SA SNT25079663SA SNT25079664SA SNT25079677SA SNT25079662SA SNT25079667SA SNT25079678SA SNT25079680SA SNT25079666SA SNT25079695SA SNT25079694SA SNT25079697SA SNT25079688SA SNT25079687SA SNT25079685SA SNT25079676SA SNT25079674SA SNT25079671SA SNT25079691SA SNT25079689SA SNT25079679SA SNT25079681SA SNT25079684SA SNT25079672SA SNT25079668SA SNT25079665SA SNT25079675SA SNT25079693SA SNT25069004SA SNT25069001SA SNT25069002SA SNT25069003SA SNT25069013SA SNT25069007SA SNT25069015SA SNT25069012SA SNT25069014SA SNT25069016SA SNT25069017SA SNT25069021SA SNT25069019SA SNT25069006SA SNT25069020SA SNT25069005SA SNT25069008SA SNT25069009SA SNT25069018SA SNT25069023SA SNT25259594SA SNT25259577SA SNT25259590SA SNT25069508SA SNT25069564SA SNT25219502SA SNT25219501SA SNT25219504SA SNT25219503SA SNT25079536SA SNT25079537SA SNT25079558SA SNT25079532SA SNT25079569SA SNT25079539SA SNT25079526SA SNT25079571SA SNT25079575SA SNT25079576SA SNT25079572SA SNT25079574SA SNT25079533SA SNT25079524SA SNT25079573SA SNT24429994SA SNT25149512SA SNT25149514SA SNT25109580SA SNT25109578SA SNT25109576SA SNT25109579SA SNT25109577SA SNT25109574SA SNT25109575SA SNT25109581SA SNT25109573SA SNT25179587SA SNT25179583SA SNT25179577SA SNT25179573SA SNT25179574SA SNT25019477SA SNT24529475SA SNT24529472SA SNT25019494SA SNT25099727SA SNT25099728SA SNT25099729SA SNT25099730SA SNT25099732SA SNT25099733SA SNT25099736SA SNT25099735SA SNT25099737SA SNT25099738SA SNT25109521SA SNT25109514SA SNT25199525SA SNT25199527SA SNT25199528SA SNT25199519SA SNT25199521SA SNT25199526SA SNT25199524SA SNT25199540SA SNT25089012SA SNT25259570SA SNT25269581SA SNT25269583SA SNT25269582SA SNT25269589SA SNT25269591SA SNT25269588SA SNT25269594SA SNT25269599SA SNT25269596SA SNT25269593SA SNT25159685SA SNT24529627SA SNT…
      status: recorded
  item list element: ListItem
    position: 9
    item:
      field: Distribution pattern
      value: Worldwide - US Nationwide distribution.
      status: recorded

enforcement-record
type: Claim
name: FDA recall Z-0453-2026: GE Healthcare Finland Oy is recalling Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE MONITOR B450 (ATO MODEL) 2068491-002 CARESCAPE MONITOR B450 B1 2107633-001 CARESCAPE MONITOR B450-GS (V2.0.8) 2094080-001
text: The FDA logged enforcement record Z-0453-2026: GE Healthcare Finland Oy is voluntarily recalling Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE MONITOR B450 (ATO MODEL) 2068491-002 CARESCAPE MONITOR B450 B1 2107633-001 CARESCAPE MONITOR B450-GS (V2.0.8) 2094080-001 — reason: Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-09-26. Affected lots/codes: UDI-DI 00840682146135 Serial numbers SNT25079613SA SNT25079608SA SNT25079622SA SNT25079618SA SNT25079619SA SNT25079614SA SNT25079611SA SNT25079621SA SNT25079620SA SNT25079603SA SNT25079616SA SNT25079612SA SNT25079602SA SNT25079615SA SNT25079663SA SNT25079664SA SNT25079677SA SNT25079662SA SNT25079667SA SNT25079678SA SNT25079680SA SNT25079666SA SNT25079695SA SNT25079694SA SNT25079697SA SNT25079688SA SNT25079687SA SNT25079685SA SNT25079676SA SNT25079674SA SNT25079671SA SNT25079691SA SNT25079689SA SNT25079679SA SNT25079681SA SNT25079684SA SNT25079672SA SNT25079668SA SNT25079665SA SNT25079675SA SNT25079693SA SNT25069004SA SNT25069001SA SNT25069002SA SNT25069003SA SNT25069013SA SNT25069007SA SNT25069015SA SNT25069012SA SNT25069014SA SNT25069016SA SNT25069017SA SNT25069021SA SNT25069019SA SNT25069006SA SNT25069020SA SNT25069005SA SNT25069008SA SNT25069009SA SNT25069018SA SNT25069023SA SNT25259594SA SNT25259577SA SNT25259590SA SNT25069508SA SNT25069564SA SNT25219502SA SNT25219501SA SNT25219504SA SNT25219503SA SNT25079536SA SNT25079537SA SNT25079558SA SNT25079532SA SNT250795…
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-0453-2026 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.