# FDA recall Z-1767-2026

> **GE Healthcare LLC** · Class II · device recall initiated 2026-02-27.

## Product

SIGNA Premier systems

## Reason for recall

Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the magnet rear and if system is accessed to perform service while the magnet is ramped, the magnetic field could attract the ferrous fittings potentially resulting in personnel injury.

## Distribution

Worldwide - US Nationwide distribution in the states of CA, MA, NJ, NY, OH, SD, TX, VA, PR and the countries of Sweden, Switzerland, United Kingdom, Vietnam, China, Norway, Portugal, Spain, France, Germany, Greece, Korea, Republic of

## Key facts

- **Recall number:** Z-1767-2026
- **Recalling firm:** GE Healthcare LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-27
- **Report date:** 2026-04-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Florence, SC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1767-2026

## Citation

> AI Analytics. FDA recall Z-1767-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1767-2026. Source: US FDA. Licensed CC0.

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