FDAJuly 14, 2022device

Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122

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

The hazard

Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.

What to do

FDA enforcement status: Completed

Brands named

philips ultrasoundphilips

UPCs

0088483810744100884838047693

Recall history

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

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Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122 — Recall Details · AllClear