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Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795116, 100-240V -, 50/60 Hz, 500 VA, CE2797, Rx Only,

FDA Recall
Terminated ·Philips Ultrasound Inc·Product code IYN·August 19, 2021

Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795090, 100-240V -, 50/60 Hz, 500 VA, CE2797, Rx Only,

FDA Recall
Terminated ·Philips Ultrasound Inc·Product code IYN·August 19, 2021

Philips Lumify Diagnostic Ultrasound, Catalogue Number: 795216 Part Number: 989605449841 with 453561845331 (software version 1.0)

FDA Recall
Terminated ·Philips Ultrasound, Inc.·Product code IYN·December 9, 2015

Transducer S8-3t UDI (01)00884838073524 REF 989605431171 Can be used as accessory with: EPIQ 7, Affiniti 70, EPIQ 5, EPIQ CVxi Ultrasound systems - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography (TEE) studies

FDA Recall
Terminated ·Philips Ultrasound Inc·Product code ITX·August 30, 2019

Philips EPIQ Diagnostic Ultrasound System, Models EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx & EPIQ CVxi - Product Usage: the systems can assist the interventionist and surgeon with image guidance during treatment of cardiovascular disease in which the procedure uses both live X-ray and live Echo Guidance.

FDA Recall
Terminated ·Philips Ultrasound Inc·Product code IYN·December 24, 2020

Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: Affiniti 30 795121 Affiniti 30 795218 Affiniti 50 795208 Affiniti 50 795118 Affiniti 70 795210 Affiniti 70 795119

FDA Recall
Completed ·Philips Ultrasound Inc·Product code IYO·August 6, 2021

3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; ClearVue 850; HD15; iU22; and Compact 5000

FDA Recall
Completed ·Philips Ultrasound, Inc.·Product code ITX·June 30, 2023

Philips X5-1 Transducer.

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code ITX·May 28, 2025

Philips L12-4 Transducer.

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code ITX·May 28, 2025

Philips L9-3 Transducer.

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code ITX·May 28, 2025

D2TCD Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

OMNI III TEE Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

C9-3v Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

C10-3v Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

D5cwc Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

C8-4v Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

BP10-5ec Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

C9-5ec Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025

SCNHD LA L7-4 HDI Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code ITX·July 3, 2025

C9-3io Transducer Probe

FDA Recall
Open, Classified ·Philips Ultrasound, Inc·Product code IYN·July 3, 2025