# FDA recall Z-0807-2024

> **Philips North America** · Class III · device recall initiated 2023-12-29.

## Product

Achieva 1.5T, Model No. 781178, 781196, 781296

## Reason for recall

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

## Distribution

Worldwide - US Nationwide distribution in the states of AR, CO, IL, MD, MS, NE, TX and the countries of Brazil, Canada, China, Germany, Greece, India, Mexico, and Saudi Arabia.

## Key facts

- **Recall number:** Z-0807-2024
- **Recalling firm:** Philips North America
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-29
- **Report date:** 2024-01-31

- **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-0807-2024

## Citation

> AI Analytics. FDA recall Z-0807-2024. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-0807-2024. Source: US FDA. Licensed CC0.

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