# FDA recall Z-1872-2024

> **Philips North America Llc** · Class II · device recall initiated 2024-04-15.

## Product

Incisive CT - Computed Tomography X-Ray System intended to produce cross-sectional images of the body. Model Number: 728144

## Reason for recall

Metal mounting box on the rotating scanner on rotor (heat change box) located within the Incisive CT system, may become compromised, resulting in potential contact with other gantry components located within the Incisive CT system during rotation.  Resulting in a fragment of a damaged component expelled at a low velocity

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1872-2024
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-15
- **Report date:** 2024-05-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1872-2024

## Citation

> AI Analytics. FDA recall Z-1872-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1872-2024. Source: US FDA. Licensed CC0.

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