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.
Read the official notice →- Date
- 2023-03-22
- Country
- United States
- Brand
- Securitas Healthcare
- Product
- Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the country of Canada.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 →- 2024-12-04
- US
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.
FDA · DeviceSecuritas Healthcare LLCWorldwide distribution - US Nationwide and the countries of Canada, Switzerland.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 →
Other drugs & medical recalls in the United States
- 2023-03-22
- US
Stryker Medical Division of Stryker Corporation recalls Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency…
Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement…
FDA · DeviceStryker Medical Division of Stryker CorporationUS Nationwide distribution in the states of NY, VA.Official notice → - US
Fenwal Inc recalls Amicus Exchange Kit Therapeutics. Component of Amicus Separator multiprocedural apheresis platform
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FDA · DeviceFenwal IncNationwide distribution. International distribution to France, Korea, Taiwan,…Official notice → - US
BioFire Diagnostics, LLC recalls In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147
Due to temperature excursions with products (products being stored outside of the required temperature specifications) that may cause a reduction in performance. The temperature excursion was as a result of shipping…
FDA · DeviceBioFire Diagnostics, LLCU.S. Nationwide distribution in the states of FL and GA.Official notice → - US
Scientia Vascular, Inc. recalls Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
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FDA · DeviceScientia Vascular, Inc.US Nationwide distribution in the states of IL, AL, FL, NC, WI, GA, SC, IN,…Official notice → - US
Synthes (USA) Products LLC recalls TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Intended for temporary fixation and stabilization of proximal femur…
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FDA · DeviceSynthes (USA) Products LLCWorldwide - US Nationwide distribution in the states of MS, OR, TX and the…Official notice → - US
Maquet Cardiovascular, LLC recalls Fusion Bioline Vascular Graft, Part number M00201503046B0
One (1) Fusion Bioline Vascular graft from lot 25162546, which failed guideline straightness testing, was intermingled with lot 25162549 and distributed to customers. Use of the affected graft may result in reduction…
FDA · DeviceMaquet Cardiovascular, LLCUS Nationwide distribution in the states of FL, IN, LA, MI, MO, NC, NV, NY,…Official notice →