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…
Read the official notice →- Date
- 2024-06-12
- Country
- United States
- Brand
- Securitas Healthcare
- Product
- 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…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Australia, 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 Details may be shortened or out of date; the official notice is the authoritative source.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 → - 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
- 2024-06-12
- US
Newport Corp recalls Newport s N-LHP-928(j) units if sold as a laser head/power supply set, and N5-LPL-944-080 and N6-LPL-944-080 if sold as a power supply…
According to 21 CFR 1040.10(f)(4), each laser system classified as a Class IIIb or IV laser product shall incorporate a key-actuated master control. The key shall be removable and the laser shall not be operable when…
- US
Ion Beam Applications S.A. recalls IBA Proton Therapy System - PROTEUS 235 - Designed to produce and deliver a proton beam for the treatment of patients with localized…
Irradiation is not interrupted when some C230 Accelerator Control Unit critical parameters are outside of the defined tolerances
FDA · DeviceIon Beam Applications S.A.Worldwide - US Nationwide distribution in the state of Virginia and the…Official notice → - US
BD SWITZERLAND SARL recalls Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of…
Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.
FDA · DeviceBD SWITZERLAND SARLWorldwide - US Nationwide distribution in the states of AR, CA, CO, IL, KS,…Official notice → - US
WAVi Co. recalls WAVi Research EEG Desktop System is comprised of the WAVi Research EEG Desktop Software with Instruction Manual and Brochure, and Heart…
Following an FDA-issued Warning Letter, the firm requested return of their research EEG system components due to the closing of their research study.
FDA · DeviceWAVi Co.US: NC, TX, IL, NV, AZ, NY, CA, MI, KS, AL, FL, MD, UT, WA, PA, GA, AR, NM,…Official notice → - US
Stryker Neurovascular recalls The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The…
Stryker Neurovascular has observed an increased frequency of PTFE coating damage occurring on the Synchro Guidewires that may be caused by the practice of backloading the guidewire through the optional introducer…
FDA · DeviceStryker NeurovascularWorldwide - US Nationwide distribution including in the states of TX, NY, MD,…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101020
It has been identified that testing documentation does not support that the syringes can successfully deliver accurate volumes across the full range of their claimed graduated capacity and may pose a risk to patient…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Canada, Panama,…Official notice →