---
title: "Incisive CT Power- Whole-body computed tomography (CT) X-Ray System Model Num... — FDA record Z-1624-2023 | Is It on Recall"
description: "Potential for Incorrect Image Orientation resulting images may be flipped or reversed result in misdiagnosis, incorrect treatment of a condition, or additional"
url: https://isitonrecall.com/recall/fda-device-z-1624-2023-incisive-ct-power-whole-body-computed-tomography-ct-x-ray-system-model-number-728148-ous/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Incisive CT Power- Whole-body computed tomography (CT) X-Ray System Model Number: 728148 (OUS) — FDA record Z-1624-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 12, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Incisive CT Power- Whole-body computed tomography (CT) X-Ray System Model Number: 728148 (OUS)
- **Reason**: Potential for Incorrect Image Orientation resulting images may be flipped or reversed result in misdiagnosis, incorrect treatment of a condition, or additional radiation exposure if a rescan is required
- **Classification**: Class II
- **Recalling firm**: PHILIPS HEADQUARTERS CAMBRIDGE
- **Quantity**: 1 unit
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1624-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1624-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: (01)00884838103467 (21) Serial Number: 102342065 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

AR, CA, OK, TX Foreign: Country Argentina Australia Austria China Colombia Czech Republic Dominican Rep France Germany Guadeloupe Hong Kong India Japan Kuwait Latvia Lithuania Netherlands Norway Portugal Romania Spain Switzerland Taiwan Thailand United Kingdom Vietnam

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arkansas](https://isitonrecall.com/state/arkansas/)
- [California](https://isitonrecall.com/state/california/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: May 31, 2023
- **Recall initiation date**: Apr 12, 2023
- **Center classification date**: May 23, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1624-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [PHILIPS HEADQUARTERS CAMBRIDGE records](https://isitonrecall.com/brand/philips-headquarters-cambridge/)