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[Recalled] Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795116, 100-240V -, 50/60 Hz, 500 VA, CE2797, Rx Only, — Battery system data issue with the ultrasound system can intermittently cause a… | FDA 2021-08-19

recall fda device united-states

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

ProductPhilips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795116, 100-240V -, 50/60 Hz, 500 VA, CE2797, Rx Only,
Brand / manufacturerPhilips Ultrasound Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0071-2022
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date19 August 2021
EAN / barcode00884838098015

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: 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.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Philips Ultrasound Inc

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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