# FDA recall Z-1417-2023

> **PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.** · Class II · device recall initiated 2023-02-20.

## Product

2D Perfusion, release R1.0.x, R1.1.x, R1.2, and R1.2.1

## Reason for recall

There are technical issues related to signal generation and processing, which can lead to inaccurate presentations.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1417-2023
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-20
- **Report date:** 2023-04-26

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1417-2023

## Citation

> AI Analytics. FDA recall Z-1417-2023. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-1417-2023. Source: US FDA. Licensed CC0.

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