Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
type: Dataset
description: FDA recall Z-1031-2026 — Securitas Healthcare LLC is recalling Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3 (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: Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
  type: MedicalDevice
  manufacturer: Securitas Healthcare LLC
claims: FDA recall Z-1031-2026: Securitas Healthcare LLC is recalling Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
claims: FDA classified recall Z-1031-2026 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-1031-2026
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-1031-2026
      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: Securitas Healthcare LLC
      status: recorded
  item list element: ListItem
    position: 6
    item:
      field: Reason
      value: Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.
      status: recorded
  item list element: ListItem
    position: 7
    item:
      field: Initiated
      value: 2025-12-08
      status: recorded
  item list element: ListItem
    position: 8
    item:
      field: Lot/code info
      value: All units of the Affected Device Models sold between January 1st, 2023 and June 26th, 2024. UDI-DI: 00840948102653; Serial Numbers: 000CCC0E68FE 000CCC0E6901 000CCC0E6907 000CCC0E68FF 000CCC0E6638 000CCC0E6905 000CCC0E68FD 000CCC0E6904 000CCC0E6908 000CCC0E69AD 000CCC0E6902 000CCC0E69AE 000CCC0E69A9 000CCC0E69A8 000CCC0E6639 000CCC0E6903 000CCC0E69AA 000CCC0E6900 000CCC0E69A6 000CCC0E6B16 000CCC0E6B0D 000CCC0E6B12 000CCC0E6B20 000CCC0E6B10 000CCC0E6B1C 000CCC0E6B21 000CCC0E6B14 000CCC0E6B0C 000CCC0E6B1A 000CCC0E6B11 000CCC0E6B1F 000CCC0E6B22 000CCC0E6B15 000CCC0E6B0E 000CCC0E6B0F 000CCC0E69A5 000CCC0E69AC 000CCC0E69A3 000CCC0E69AB 000CCC0E69A4 000CCC0E6B17 000CCC0E6B19 000CCC0E6B0B 000CCC0E6B1E 000CCC0E6B13 000CCC0E6B18 000CCC0E6B1D 000CCC0E6B1B 000CCC0E6ACA 000CCC0E6ACB 000CCC0E6ABF 000CCC0E6AC4 000CCC0E6AAF 000CCC0E6ABB 000CCC0E6AB8 000CCC0E6ABD 000CCC0E6AB7 000CCC0E6ABE 000CCC0E6AC2 000CCC0E6ABA 000CCC0E6A5D 000CCC0E6A74 000CCC0E6A61 000CCC0E6A57 000CCC0E6A58 000CCC0E6A5C 000CCC0E6A62 000CCC0E6A79 000CCC0E6A6F 000CCC0E6A5B 000CCC0E6A5E 000CCC0E6A59 000CCC0E6A78 000CCC0E6B2C 000CCC0E6B26 000CCC0E6B24 000CCC0E6B35 000CCC0E6B3A 000CCC0E6B28 000CCC0E6B2E 000CCC0E6B29 000CCC0E6B31 000CCC0E6B23 000CCC0E6B2A 000CCC0E6B34 000CCC0E6B38 000CCC0E6B36 000CCC0E6B27 000CCC0E6B33 000CCC0E6B39 000CCC0E6B25 000CCC0E6B2D 000CCC0E6B2B 000CCC0E6B32 000CCC0E6B2F 000CCC0E6B37 000CCC0E6B30 000CCC0E6A6C 000CCC0E6A6B 000CCC0E6948 000CCC0E6A67 000CCC0E6637 000CCC0E6946 000CCC0E6945 000CCC0E6947 000CCC0E6A68 000CCC0E6636 000CCC0E6A66 000CCC0E694D 000CCC0E6949 000CCC0E6A63 000CCC0E694F 000CCC0E694B 000CCC0E6A6D 000CCC0E6A69 000CCC0E694C 000CCC0E6A65 000CCC0E6A6A 000CCC0E6950 000CCC0E6A6E 000CCC0E694A 000CCC0E6A1E 000CCC0E6A50 000CCC0E6A24 000CCC0E6A4F 000CCC0E6A1F 000CCC0E6AD2 000CCC0E6A25 000CCC0E6A4C 000CCC0E6AD4 000CCC0E6AD7 000CCC0E6AC6 000CCC0E6ACD 000CCC0E6AC3 000CCC0E6ACE 000CCC0E6AC8 000CCC0E6AD9 000CCC0E6ADA 000CCC0E6AD0 000CCC0E6AD5 000CCC0E6AD8 000CCC0E6ACC 000CCC0E6AC7 000CCC0E6…
      status: recorded
  item list element: ListItem
    position: 9
    item:
      field: Distribution pattern
      value: Worldwide distribution -US Nationwide and the country of Canada.
      status: recorded

FDA recall Z-1031-2026: Securitas Healthcare LLC is recalling Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
type: Claim
text: The FDA logged enforcement record Z-1031-2026: Securitas Healthcare LLC is voluntarily recalling Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3 — reason: Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-12-08. Affected lots/codes: All units of the Affected Device Models sold between January 1st, 2023 and June 26th, 2024. UDI-DI: 00840948102653; Serial Numbers: 000CCC0E68FE 000CCC0E6901 000CCC0E6907 000CCC0E68FF 000CCC0E6638 000CCC0E6905 000CCC0E68FD 000CCC0E6904 000CCC0E6908 000CCC0E69AD 000CCC0E6902 000CCC0E69AE 000CCC0E69A9 000CCC0E69A8 000CCC0E6639 000CCC0E6903 000CCC0E69AA 000CCC0E6900 000CCC0E69A6 000CCC0E6B16 000CCC0E6B0D 000CCC0E6B12 000CCC0E6B20 000CCC0E6B10 000CCC0E6B1C 000CCC0E6B21 000CCC0E6B14 000CCC0E6B0C 000CCC0E6B1A 000CCC0E6B11 000CCC0E6B1F 000CCC0E6B22 000CCC0E6B15 000CCC0E6B0E 000CCC0E6B0F 000CCC0E69A5 000CCC0E69AC 000CCC0E69A3 000CCC0E69AB 000CCC0E69A4 000CCC0E6B17 000CCC0E6B19 000CCC0E6B0B 000CCC0E6B1E 000CCC0E6B13 000CCC0E6B18 000CCC0E6B1D 000CCC0E6B1B 000CCC0E6ACA 000CCC0E6ACB 000CCC0E6ABF 000CCC0E6AC4 000CCC0E6AAF 000CCC0E6ABB 000CCC0E6AB8 000CCC0E6ABD 000CCC0E6AB7 000CCC0E6ABE 000CCC0E6AC2 000CCC0E6ABA 000CCC0E6A5D 000CCC0E6A74 000CCC0E6A61 000CCC0E6A57 000CCC0E6A58 000CCC0E6A5C 000CCC0E6A62 000CCC0E6A79 000CCC0E6A6F 000CCC0E6A5B 000CCC0E6A5E 000CCC0E6A59 000CCC0E6A78 000CCC0E6B2C 000CCC0E6B26 000CCC0E6B24 000CCC0E6B35 000CCC0E6B3A 000CCC0E6B28 000CCC0E6B2E 000CCC0E6B29 000CCC0E6B31 000CCC0E6B23 000CCC0E6B2A 000CCC0E6B34 000CCC0E6B38 000CCC0E6B36 000CCC0E6B27 000CCC0E6B33 000CCC0E6B39 000CCC0E6…
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-1031-2026 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.