# FDA recall Z-1806-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-04-07.

## Product

Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.

## Reason for recall

If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.

## Distribution

Worldwide distribution - US Nationwide distribution including the states of CA, ME, RI, TX, WI and the countries of Canada,   Australia, Austria, France, Germany, Greece, Hungary, Ireland, Netherlands, Portugal, Slovenia, United Kingdom.

## Key facts

- **Recall number:** Z-1806-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-07
- **Report date:** 2020-05-06
- **Termination date:** 2023-04-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1806-2020

## Citation

> AI Analytics. FDA recall Z-1806-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1806-2020. Source: US FDA. Licensed CC0.

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