# FDA recall Z-1554-2025

> **Philips North America Llc** · Class II · device recall initiated 2025-03-10.

## Product

Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.

## Reason for recall

Potential for collimator to fall as a result of incorrect installation.

## Distribution

Worldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH, NY, OR, PA, TX, WI and the countries of Argentina, Australia, Canada, Chile, China, Germany, Hungary, India, Indonesia, Italy, Kenya, Mexico, Netherlands, New Zealand, Oman, Pakistan, Peru, Poland, Romania, Russian Federation, Slovenia, South Africa, Spain, Thailand, United Kingdom, Vietnam.

## Key facts

- **Recall number:** Z-1554-2025
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-10
- **Report date:** 2025-04-23

- **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-1554-2025

## Citation

> AI Analytics. FDA recall Z-1554-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1554-2025. Source: US FDA. Licensed CC0.

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