Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c recall — FDA Z-1007-2026
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
Overview of recall records associated with Philips Ultrasound, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
This page summarizes recall records in which the official source identifies Philips Ultrasound, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.