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FDAAugust 19, 2021device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

philips ultrasoundphilips

UPCs

0088483809797100884838028098

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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