Arial 900 MHz Call Station
Medical device recall Z-1032-2026. Published in FDA’s Enforcement Report on Jan 14, 2026.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jan 14, 2026. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 1898 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3
1898 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
All units of the Affected Device Models sold between January 1st, 2023 and June 26th, 2024. UDI-DI: 00840948102660; Serial Numbers:000CCC0E6CC9 000CCC0E6CC6 000CCC0E6CCC 000CCC0E6CCE 000CCC0E6CC5 000CCC0E6CD0 000CCC0E6D1F 000CCC0E6D1B…
Every code shown here, 1,990 characters
All units of the Affected Device Models sold between January 1st, 2023 and June 26th, 2024. UDI-DI: 00840948102660; Serial Numbers:000CCC0E6CC9 000CCC0E6CC6 000CCC0E6CCC 000CCC0E6CCE 000CCC0E6CC5 000CCC0E6CD0 000CCC0E6D1F 000CCC0E6D1B 000CCC0E6D24 000CCC0E6D1C 000CCC0E6D22 000CCC0E6D01 000CCC0E6D04 000CCC0E6D19 000CCC0E6D1A 000CCC0E6D1E 000CCC0E6CC8 000CCC0E6D23 000CCC0E6CCD 000CCC0E6D1D 000CCC0E6CCB 000CCC0E6CCA 000CCC0E6CC7 000CCC0E6D20 000CCC0E6CCF 000CCC0E627E 000CCC0E6286 000CCC0E628C 000CCC0E6282 000CCC0E627C 000CCC0E6279 000CCC0E6289 000CCC0E627A 000CCC0E628E 000CCC0E627D 000CCC0E6288 000CCC0E6280 000CCC0E6284 000CCC0E6DDB 000CCC0E6D2E 000CCC0E6D28 000CCC0E6DE0 000CCC0E6D27 000CCC0E6D2C 000CCC0E6D2F 000CCC0E6DE3 000CCC0E6D2D 000CCC0E6D30 000CCC0E6DE1 000CCC0E6DD9 000CCC0E6DDF 000CCC0E6D25 000CCC0E6DDE 000CCC0E6DE4 000CCC0E6D2A 000CCC0E6D2B 000CCC0E6D29 000CCC0E6DDC 000CCC0E6DDA 000CCC0E6D26 000CCC0E6D36 000CCC0E6D32 000CCC0E6D06 000CCC0E6D33 000CCC0E6D3C 000CCC0E6D38 000CCC0E6D3B 000CCC0E6D07 000CCC0E6D05 000CCC0E6D0B 000CCC0E6D0A 000CCC0E6D0C 000CCC0E6D03 000CCC0E6D37 000CCC0E6D31 000CCC0E6D39 000CCC0E6D35 000CCC0E6D3A 000CCC0E6D34 000CCC0E6D08 000CCC0E6341 000CCC0E6D02 000CCC0E6D09 000CCC0E5B9F 000CCC0E5BD5 000CCC0E5BE0 000CCC0E6719 000CCC0E676D 000CCC0E676E 000CCC0E6DE2 000CCC0E6DDD 000CCC0E6CBC 000CCC0E6CC0 000CCC0E6CBF 000CCC0E6CBB 000CCC0E6CB9 000CCC0E6CBA 000CCC0E6D6A 000CCC0E6CC2 000CCC0E6CBE 000CCC0E6D61 000CCC0E6D67 000CCC0E6D68 000CCC0E6D62 000CCC0E6CC1 000CCC0E6D65 000CCC0E6D63 000CCC0E6CC3 000CCC0E6D66 000CCC0E6CBD 000CCC0E6CC4 000CCC0E6D64 000CCC0E6D69 000CCC0E6D6C 000CCC0E6D6B 000CCC0E6483 000CCC0E6482 000CCC0E647D 000CCC0E62A2 000CCC0E6484 000CCC0E633D 000CCC0E647A 000CCC0E647B 000CCC0E6340 000CCC0E6480 000CCC0E6481 000CCC0E647E 000CCC0E633C 000CCC0E62B6 000CCC0E647F 000CCC0E647C 000CCC0E6342 000CCC0E6343 000CCC0E633A 000CCC0E6479 000CCC0E6271 000CCC0E6278 000CCC0E6270 000CCC0E635C 000CCC0E6354 000CCC0E6353 000CCC0E6275 000CCC0E6355…
FDA’s list runs to 24,804 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide distribution -US Nationwide and the country of Canada.
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Dec 8, 2025.
- FDA classified it on Jan 8, 2026.
- FDA’s Enforcement Report published it on Jan 14, 2026.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Securitas Healthcare LLC, of Lincoln, NE.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 24,804 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.