# FDA recall Z-1585-2023

> **Philips North America** · Class II · device recall initiated 2023-03-20.

## Product

Philips Incisive CT -Computed Tomography X-Ray System  Model Number: 72814

## Reason for recall

Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury

## Distribution

Worldwide - US Nationwide distribution in the states of AR, CA, FL, IL, IN, MI, MO, NY, TN,  TX, VT and the countries of Australia, Chile, Costa Rica, Czech Republic, Dominican, Republic Germany, India, Israel, Japan, Lithuania, Philippines, Poland, Sint Maarten (Dutch part), South Africa, Thailand, United Kingdom, Utd. Arab. Emir.

## Key facts

- **Recall number:** Z-1585-2023
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-20
- **Report date:** 2023-05-24

- **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-1585-2023

## Citation

> AI Analytics. FDA recall Z-1585-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1585-2023. Source: US FDA. Licensed CC0.

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