# FDA recall Z-1477-2023

> **Philips North America Llc** · Class II · device recall initiated 2022-10-21.

## Product

Philips ProxiDiagnost N90 1.0 (Model 706100) and  ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general radiography and fluoroscopy (R/F) system

## Reason for recall

Potential table stop due to a broken tabletop cable:  On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking

## Distribution

Worldwide distribution - US Nationwide including Puerto Rico and the countries of Australia, Chile, China, Germany, India, Italy, Malaysia, Netherlands, Panama, Spain,  Thailand.

## Key facts

- **Recall number:** Z-1477-2023
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-21
- **Report date:** 2023-05-10

- **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-1477-2023

## Citation

> AI Analytics. FDA recall Z-1477-2023. Retrieved 2026-08-02 from https://api.ai-analytics.org/recall/Z-1477-2023. Source: US FDA. Licensed CC0.

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