# FDA recall Z-1073-2024

> **Philips North America** · Class II · device recall initiated 2023-12-15.

## Product

ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system  Ref:706150

## Reason for recall

Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patients radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image.  Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)

## Distribution

Nationwide Foreign: Australia Germany India Italy Malaysia Panama Thailand

## Key facts

- **Recall number:** Z-1073-2024
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-15
- **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-1073-2024

## Citation

> AI Analytics. FDA recall Z-1073-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1073-2024. Source: US FDA. Licensed CC0.

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