# FDA recall Z-0241-2026

> **PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.** · Class II · device recall initiated 2025-09-29.

## Product

Zenition 50;  Product Number (REF): 718096; Interventional fluoroscopic x-ray system

## Reason for recall

Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV) control board.

## Distribution

Distribution US states of MO and TX; Belgium, Canada, Fiji, Germany, India, Malaysia, Mexico, Morocco, South Africa, South Korea, Thailand, United Kingdom, and Uzbekistan.

## Key facts

- **Recall number:** Z-0241-2026
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-29
- **Report date:** 2025-10-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Best, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0241-2026

## Citation

> AI Analytics. FDA recall Z-0241-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-0241-2026. Source: US FDA. Licensed CC0.

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