44 results · 14ms · Sources: EU EUDAMED, US FDA

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Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·September 25, 2023

Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360; mobile patient alarm

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·September 25, 2023

Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·December 8, 2025

Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·December 8, 2025

Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·June 20, 2024

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 Arial Emergency and Nurse Call System.

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·April 11, 2024

Arial Water Resistant Pendant with Long Wristband, Models: 59362 and 2560-59362; mobile patient alarm

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·September 25, 2023

Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·June 20, 2024

Ascom Telligence Nurse Call System

FDA Recall
Open, Classified ·Ascom (US) Inc.·Product code IQA·November 2, 2018

Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·February 6, 2023

Senior Living Arial Emergency and Nurse Call Systems

FDA Recall
Open, Classified ·Stanley Security Solutions Inc·Product code IQA·November 17, 2021

Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Arial Care Giver Application

FDA Recall
Open, Classified ·Securitas Healthcare LLC·Product code IQA·November 1, 2024

1.5T SIGNA Excite HD, 3.0T SIGNA Excite HD. Magnetic Resonance Imaging System

FDA Recall
Open, Classified ·GE Healthcare, LLC·Product code LNH·February 18, 2022

Signa 1.5T TwinSpeed Magnetic Resonance Imaging System

FDA Recall
Open, Classified ·GE Healthcare, LLC·Product code LNH·February 18, 2022

SIGNA Excite 3T. Magnetic Resonance Imaging System

FDA Recall
Open, Classified ·GE Healthcare, LLC·Product code LNH·February 18, 2022

1.5T and 3.0T SIGNA HDx, 1.5T and 3.0T SIGNA HDxt, and 1.5T SIGNA HDxt Mobile. Magnetic Resonance Imaging System

FDA Recall
Open, Classified ·GE Healthcare, LLC·Product code LNH·February 18, 2022

myQA iON; Article Number: MQ10-000;

FDA Recall
Open, Classified ·IBA Dosimetry GmbH Bahnhofstr. 5 Schwarzenbruck Germany·Product code IYE·April 1, 2025

RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d) 170065 e) 170070 f) 170075 g) 170080 h) 170085 i) 170090 j) 170095

FDA Recall
Open, Classified ·Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland·Product code BTR·July 16, 2021

RUSCH Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF numbers: a) 112080050 b) 112080055 c) 112080060 d) 112080065 e) 112080070 f) 112080075 g) 112080080 h) 112080085 i) 112080090 j) 112080095 k) 112080100

FDA Recall
Open, Classified ·Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland·Product code BTR·July 16, 2021

RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100

FDA Recall
Open, Classified ·Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland·Product code BTR·July 16, 2021