No image published for this recall

No image published for this recall

Philips Ingenuity Core128 Model # 728323, computed tomography x-ray system - safety alert

Official notice

14 Aug 2019

Last checked

14 Aug 2019

Medium riskFDA

An official FDA notice concerns Philips Ingenuity Core128 Model # 728323, computed tomography x-ray system - safety alert. An official FDA notice concerns Ingenuity Core128 Model # 728323, computed tomography x-ray system. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-08-14. Recall numbers: Z-2187-2019. Check the official notice for the complete list. Published 2019-08-14.

What to do now

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

Units affected

116

Recall number

Z-2187-2019

Official notice

2019-08-14

The hazard

An official FDA notice concerns Ingenuity Core128 Model # 728323, computed tomography x-ray system. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-08-14. Recall numbers: Z-2187-2019. 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

83365

Recall Numbers

Z-2187-2019

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Affected products

Product 1

Ingenuity Core128 Model # 728323, computed tomography x-ray system

Units affected

116

Risk / hazard

An official FDA notice concerns Ingenuity Core128 Model # 728323, computed tomography x-ray system. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-08-14. Recall numbers: Z-2187-2019. 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 · OH · Cleveland

Affected area 1

US · United States · OH · Cleveland

Affected area 2

US · United States

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Philips. Contact: Philips Medical Systems (Cleveland) Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2187-2019

Event id

83365

Units affected

116

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA5 Nov 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA19 Nov 2025
US
No image published for this recall

Pinnacle 3 with TumorLOC, (870258) Radiation Therapy Planning System Software - safety alert

Medium riskFDA13 Aug 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA28 May 2025
US
No image published for this recall

Cardiac Workstation 5000; Model Number: 860439 - safety alert

Medium riskFDA22 Oct 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA30 Apr 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA7 Jan 2026
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA17 Dec 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA10 Dec 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA10 Dec 2025
US
No image published for this recall

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841, - safety alert

Medium riskFDA10 Dec 2025
US
No image published for this recall

ProxiDiagnost N90; Model Number: 706110 - safety alert

Medium riskFDA19 Nov 2025

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 14 Aug 2019. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.