437 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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BrightView XCT, Gamma Camera, Product Code 882482
FDA Recall
Open, Classified
·Philips North America·Product code KPS·November 30, 2023
BrightView, Gamma Camera System, Product Code 882480.
FDA Recall
Open, Classified
·Philips North America·Product code KPS·November 30, 2023
BrightView X, Gamma Camera, Product Code 882478
FDA Recall
Open, Classified
·Philips North America·Product code KPS·November 30, 2023
Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Systems for use as a diagnostic device.
FDA Recall
Open, Classified
·Philips North America Llc·Product code LNH·November 17, 2023
DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system. Model: RGD2461AMI Philips Part # 866126
FDA Recall
Open, Classified
·Philips North America Llc·Product code MHX·February 15, 2024
CombiDiagnost R90; Model Number: 709031;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code KPR·October 1, 2025
Radiography 7300 C; Model Number: 712037;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code KPR·October 1, 2025
ProxiDiagnost N90; Model Number: 706110;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025
Precision CRF; Model Number: 706400;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025
IntelliVue Patient Monitor MX500 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866064. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates.
FDA Recall
Open, Classified
·Philips North America Llc·Product code MHX·June 28, 2024
IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866062. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates.
FDA Recall
Open, Classified
·Philips North America Llc·Product code MHX·June 28, 2024
IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866066. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates.
FDA Recall
Open, Classified
·Philips North America Llc·Product code MHX·June 28, 2024
IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866060. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates.
FDA Recall
Open, Classified
·Philips North America Llc·Product code MHX·June 28, 2024
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code MQB·October 1, 2025
Achieva XR. Model (REF) Numbers 781153, 781253.
FDA Recall
Open, Classified
·Philips North America·Product code LNI·January 3, 2024
Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
FDA Recall
Open, Classified
·Philips North America·Product code LNI·January 3, 2024
Achieva 1.5T Initial system. Model (REF) Numbers 781178.
FDA Recall
Open, Classified
·Philips North America·Product code LNI·January 3, 2024
Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
FDA Recall
Open, Classified
·Philips North America·Product code LNI·January 3, 2024
SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.
FDA Recall
Open, Classified
·Philips North America·Product code LNI·January 3, 2024