Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number 712211) DuraDiagnost (R3.0, Product Number 712211)
Reported: June 21, 2017 Initiated: May 31, 2017 #Z-2322-2017
Product Description
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
Details
- Recalling Firm
- Philips Electronics North America Corporation
- Units Affected
- 98 sytems
- 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.
- Location
- Andover, MA
Frequently Asked Questions
What product was recalled? ▼
Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number 712211) DuraDiagnost (R3.0, Product Number 712211). Recalled by Philips Electronics North America Corporation. Units affected: 98 sytems.
Why was this product recalled? ▼
Tube arm assembly could fall down due to cracked welding joints
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 21, 2017. Severity: Moderate. Recall number: Z-2322-2017.
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