medical Class II Updated 2021-08-25

Philips Ultrasound Inc recalls EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C

Recalled Product

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi


Hazard / Issue

Ultrasound system control panel arm swivel lock could fail, which could cause the control panel and monitor to swivel freely while a user is positioning the monitor, or transporting/moving the system, which could lead to patient or user musculoskeletal injury.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Manufactured Between 2020-02-27 to 2021-05-25
View official government recall

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