# FDA recall Z-1933-2025

> **Philips North America** · Class II · device recall initiated 2025-05-29.

## Product

Intera 1.5T Master/Nova  Product Number: 781106;

## Reason for recall

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

## Distribution

Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador, Germany, Iran, Italy, Japan, Lebanon, Libya,  Mexico, Poland, Portugal, Spain.

## Key facts

- **Recall number:** Z-1933-2025
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-29
- **Report date:** 2025-06-18

- **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-1933-2025

## Citation

> AI Analytics. FDA recall Z-1933-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1933-2025. Source: US FDA. Licensed CC0.

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