FDA Device Intelligence
Home › VIASONIX LTD › Dolphin/XF Robot Accessory

Dolphin/XF Robot Accessory

VIASONIX LTD · Model Dolphin/XF Robot Accessory · UDI-DI 07290016880229

IYNITXOQQ Prescription
1
510(k) clearances
2,691
Adverse events (35 deaths)
298
Recalls
221
Facilities

Description

The Dolphin/XF robot accessory, when used with the Dolphin system, is a device which assists the user in the acquisition of cerebral blood flow velocity

Recalls

DateFirmReason
2025-10-31Philips Ultrasound, LLCUltrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-09-18GE Medical Systems, LLCThe Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinica
2025-09-18GE Medical Systems, LLCThe Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinica
2025-09-18GE Medical Systems, LLCThe Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinica

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.