Securitas Healthcare LLC recalls Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Arial Care Giver…
Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.
Read the official notice →- Date
- 2024-12-04
- Country
- United States
- Brand
- Securitas Healthcare
- Product
- Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Arial Care Giver…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Canada, Switzerland.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Securitas Healthcare recalls
- 2026-01-14
USSecuritas Healthcare LLC recalls Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3
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…
FDA · DeviceSecuritas Healthcare LLCWorldwide distribution -US Nationwide and the country of Canada.Official notice →- 2024-07-31
- US
Securitas Healthcare LLC recalls Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.
This is a risk that alarms will not be received by the Arial Wireless Nurse Call System and premature depletion of the battery.
FDA · DeviceSecuritas Healthcare LLCUS: FL, CA, AL, ND, MS, WA, MN, TX, OR, WI, MD, NY, NEOfficial notice → - US
Securitas Healthcare LLC recalls Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living…
There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.
FDA · DeviceSecuritas Healthcare LLCUS: NE, MN, WA, MD, TX, ON, WI, OR, MS, CA, and CanadaOfficial notice → - 2024-06-12
- US
Securitas Healthcare LLC recalls Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that utilizes Apple iOS 17.4 and Apple iOS 17.5, a component of the…
The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is frequently restarting causing the app to receive alerts for all pending alarm notifications and other events when the app restarts, experience…
FDA · DeviceSecuritas Healthcare LLCWorldwide distribution - US Nationwide and the countries of Australia, Canada,…Official notice → - 2023-11-15
- US
Securitas Healthcare LLC recalls Arial Water Resistant Pendant with Long Wristband, Models: 59362 and 2560-59362; mobile patient alarm
Premature battery depletion presents a risk that alarms will not be received by the Arial Wireless Emergency Call System.
FDA · DeviceSecuritas Healthcare LLCWorldwide distribution - US Nationwide and the country of Canada.Official notice → - 2023-03-22
- US
Securitas Healthcare LLC recalls Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial…
The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices.
FDA · DeviceSecuritas Healthcare LLCWorldwide distribution - US Nationwide and the country of Canada.Official notice →
Other drugs & medical recalls in the United States
- 2024-12-04
- US
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LivaNova Deutschland GmbH recalls Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software
Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds, safety/performance functions remain operational before reset, control maintained through backup control panel, but second reset may occur, may lead to…
FDA · DeviceLivaNova Deutschland GmbHUS Nationwide distribution in the states of CA, VA, GA, IN, NJ, FL, CO, MS, NV.Official notice → - US
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
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MEDLINE INDUSTRIES, LP - Northfield recalls ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use…
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Remote Diagnostic Technologies Ltd. recalls Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or…
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