# FDA recall Z-0679-2024

> **Philips North America** · Class II · device recall initiated 2023-11-30.

## Product

BrightView XCT, Gamma Camera, Product Code 882482

## Reason for recall

While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created between the patient support and the detector, which may present a potential extremity entrapment hazard. Risk to patients may include fracture, body part loss of function/debilitation, muscle or ligament sprain or strain, laceration, crush injury, abrasion, or  contusion.

## Distribution

Domestic distribution nationwide. Foreign distribution worldwide.

## Key facts

- **Recall number:** Z-0679-2024
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-30
- **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-0679-2024

## Citation

> AI Analytics. FDA recall Z-0679-2024. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-0679-2024. Source: US FDA. Licensed CC0.

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