Philips Ultrasound Inc: Medical Device Recall in 2021 - (Recall #: Z-0071-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 19, 2021

Date Posted: October 13, 2021

Recall Number: Z-0071-2022

Event ID: 88625

Reason for Recall:

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.

Status: Terminated

Product Quantity: 1 unit

Code Information:

Affected Serial Number/UDI numbers: US92010594 (01)00884838098015(21)US92010594

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of CA, MA, MD, MI, MS, NC, NY, OH, VA, WA and the countries of Australia, Portugal, Netherlands, Canada, Netherlands, Germany.

Voluntary or Mandated:

Voluntary: Firm initiated