# FDA recall Z-1087-2024

> **PHILIPS MEDICAL SYSTEMS** · Class II · device recall initiated 2022-02-11.

## Product

CombiDiagnost R90 1.0 (709030)

## Reason for recall

While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.

## Distribution

US Nationwide distribution in the states of CA, FL, GA, IL, IN, KS, MD, ME, MI, MN, NC, NJ, NY, TX, VA, WA.

## Key facts

- **Recall number:** Z-1087-2024
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-02-11
- **Report date:** 2024-02-21

- **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-1087-2024

## Citation

> AI Analytics. FDA recall Z-1087-2024. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1087-2024. Source: US FDA. Licensed CC0.

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