# FDA recall Z-1003-2026

> **Philips Healthcare (Suzhou) Co., Ltd.** · Class II · device recall initiated 2025-12-03.

## Product

Philips Incisive CT

## Reason for recall

Potential for incomplete scan due to unstable connection inside of floating sensor.

## Distribution

U.S. and U.S. territories

## Key facts

- **Recall number:** Z-1003-2026
- **Recalling firm:** Philips Healthcare (Suzhou) Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-03
- **Report date:** 2026-01-14

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Suzhou, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1003-2026

## Citation

> AI Analytics. FDA recall Z-1003-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1003-2026. Source: US FDA. Licensed CC0.

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