# FDA recall Z-0715-2024

> **Philips North America** · Class II · device recall initiated 2021-07-15.

## Product

(1) Ingenia Ambition X (Product Number 781356);  (2) Ingenia Ambition S (Product Number 781359)

## Reason for recall

The sealed magnet will experience uncontrolled shutdown known as Loss-of-Field (LoF) if the magnet loses cryo-cooling (e.g. caused by a power outage on site.)

## Distribution

Domestic distribution to the following states and territories: CA DE FL GA IL KY MA ME MI MO NH NJ NM NY OH PA SC TN TX VA VT WI WY, and PR.  International distribution worldwide.

## Key facts

- **Recall number:** Z-0715-2024
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-07-15
- **Report date:** 2024-01-17

- **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-0715-2024

## Citation

> AI Analytics. FDA recall Z-0715-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0715-2024. Source: US FDA. Licensed CC0.

---

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