No image published for this recall

No image published for this recall

Philips EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi - safety alert

Official notice

25 Aug 2021

Last checked

25 Aug 2021

Critical riskFDA

An official FDA notice concerns Philips EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi - safety alert. An official FDA notice concerns EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi. The notice reports a chemical exposure risk. Stop using the product and follow the official notice. Published 2021-08-25. Recall numbers: Z-2306-2021. Check the official notice for the complete list. Published 2021-08-25.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

8,935

Recall number

Z-2306-2021

Official notice

2021-08-25

The hazard

An official FDA notice concerns EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi. The notice reports a chemical exposure risk. Stop using the product and follow the official notice. Published 2021-08-25. Recall numbers: Z-2306-2021. Check the official notice for the complete list.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

88313

Recall Numbers

Z-2306-2021

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Affected products

Product 1

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

Units affected

8,935

Risk / hazard

An official FDA notice concerns EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi. The notice reports a chemical exposure risk. Stop using the product and follow the official notice. Published 2021-08-25. Recall numbers: Z-2306-2021. Check the official notice for the complete list.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · WA · Bothell

Affected area 1

US · United States · WA · Bothell

Affected area 2

US · United States

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Philips. Contact: Philips Ultrasound Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

critical

Recall details

Recall number

Z-2306-2021

Event id

88313

Units affected

8,935

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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