# FDA recall Z-2402-2025

> **Philips Ultrasound, Inc** · Class III · device recall initiated 2025-07-03.

## Product

TRANSDUCER L12-5 Transducer Probe

## Reason for recall

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2402-2025
- **Recalling firm:** Philips Ultrasound, Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-03
- **Report date:** 2025-09-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Reedsville, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2402-2025

## Citation

> AI Analytics. FDA recall Z-2402-2025. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2402-2025. Source: US FDA. Licensed CC0.

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