# FDA recall Z-1850-2024

> **Philips North America Llc** · Class II · device recall initiated 2024-05-03.

## Product

Ingenia Ambition S  Model Number (REF):   (1) 782139;  (2) 782133;  (3) 782108;  (4) 781359

## Reason for recall

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's  technical room, resulting in Smoke and/or fire

## Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Canada,  China, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Italy, Japan,  Lebanon, Libya, Lithuania, Martinique, Netherlands, Norway, Poland, Romania, Slovakia,  Spain, Sweden, Switzerland, Thailand, United Kingdom.

## Key facts

- **Recall number:** Z-1850-2024
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-03
- **Report date:** 2024-05-29

- **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-1850-2024

## Citation

> AI Analytics. FDA recall Z-1850-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1850-2024. Source: US FDA. Licensed CC0.

---

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