device · product 1 of 1
Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number 712211) DuraDiagnost (R3.0, Product Number 712211)
- Recall number
- Z-2322-2017
- Initiated
- May 31, 2017
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Philips Electronics North America Corporation
- Quantity
- 98 sytems
App-derived interpretation
Tube arm assembly could fall down due to cracked welding joints
Official device-enrichment evidence · Sourced
Device Design
Inspect official wording and provenance
Reason for recall
Tube arm assembly could fall down due to cracked welding joints
Code information
SN120001-SN120003, SN130001-SN130023, SN140001-SN140022, SN140024, SN140027, SN140030-SN140031, SN140033-SN140046, SN140048, SN140050-SN140068, SN150001-SN150004, SN150006, SN150008-SN150011, SN160001, SN160002
Distribution pattern
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.