# FDA recall Z-1252-2025

> **Philips Medical Systems Nederland B.V.** · Class II · device recall initiated 2024-04-04.

## Product

Philips IntelliSpace Cardiovascular software, Model 830089.

## Reason for recall

Study data is not able to be archived, copied, or exported with the cardiovascular software version.

## Distribution

US Nationwide distribution in the states of AK, AL, AZ, CA, CT, FL, GA, IA, IN, KY, MA, MI, MN, NC, NE, NY, OH, OR, TN, TX, VA, and WI.  There was government distribution but no military distribution.

## Key facts

- **Recall number:** Z-1252-2025
- **Recalling firm:** Philips Medical Systems Nederland B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-04
- **Report date:** 2025-03-12

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1252-2025

## Citation

> AI Analytics. FDA recall Z-1252-2025. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-1252-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*