# FDA recall Z-2322-2017

> **Philips Electronics North  America Corporation** · Class II · device recall initiated 2017-05-31.

## Product

Philips DuraDiagnost X-ray systems:   DuraDiagnost (R1.0, Product Number 712210)  DuraDiagnost (R2.0, Product Number 712211)  DuraDiagnost (R3.0, Product Number 712211)

## Reason for recall

Tube arm assembly could fall down due to cracked welding joints

## Distribution

Worldwide Distribution - US Distribution to the states of : Ca and Oh., and to the countries of: Australia, Libya, China, Mayotte, Mexico, France, United Kingdom, Germany,  Ecuador, Australia, Spain, Switzerland, Macedonia, Uzbekistan, Kuwait, Malaysia, Netherlands, Argentina,  Chile, Colombia, Egypt, United Arab Emirates, Saudi Arabia, Hungary, Peru, Poland, Indonesia, Burkina Faso, Kazakhstan, Turkey and Slovenia.

## Key facts

- **Recall number:** Z-2322-2017
- **Recalling firm:** Philips Electronics North  America Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-31
- **Report date:** 2017-06-21
- **Termination date:** 2018-08-24

- **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-2322-2017

## Citation

> AI Analytics. FDA recall Z-2322-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2322-2017. Source: US FDA. Licensed CC0.

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