Philips Electronics North America Corporation: Medical Device Recall in 2017 - (Recall #: Z-2322-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

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)

Product Classification:

Class II

Date Initiated: May 31, 2017

Date Posted: June 21, 2017

Recall Number: Z-2322-2017

Event ID: 77410

Reason for Recall:

Tube arm assembly could fall down due to cracked welding joints

Status: Terminated

Product Quantity: 98 sytems

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.

Voluntary or Mandated:

Voluntary: Firm initiated