Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips DuraDiagnost X-Ray system Recalled by Philips Medical Systems, Inc. Due to Improper installation of Tube arm, and Wall stand...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems, Inc. directly.
Affected Products
Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
Quantity: 71 units
Why Was This Recalled?
Improper installation of Tube arm, and Wall stand may cause it to fall down, Improper installation of table may cause it to float.
Where Was This Sold?
Worldwide Distribution. Argentina, Australia, Burkina-Faso, Chile, China, Colombia, Ecuador, France, Germany, Hungary, Indonesia, Iraq (NL), Kuwait, Libya, Macedonia, Malaysia, Mayotte, Poland, Saudi Arabia, Slovenia, Spain, Switzerland, Turkey, United Kingdom, and Uzbekistan.
About Philips Medical Systems, Inc.
Philips Medical Systems, Inc. has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report