medical Class II Updated 2021-10-13

Philips Ultrasound Inc recalls Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System

Recalled Product

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


Hazard / Issue

Battery system data issue with the ultrasound system can intermittently cause a system shutdown, regardless of actual battery state or application of alternating current power.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Affected Serial Number/UDI numbers: US92010594 (01)00884838098015(21)US92010594
View official government recall

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