Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips BuckyDiagnost Radiographic Recalled by Philips Healthcare Inc. Due to An inspection shows several IATDs (Installation Acceptance Test...
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 Healthcare Inc. directly.
Affected Products
Philips BuckyDiagnost Radiographic, a Diagnostic X-ray system. Catalog Numbers: 704031, 704032, 704035, 704060, 704062 This system is used for making x-ray exposures for diagnostics.
Quantity: 66 units
Why Was This Recalled?
An inspection shows several IATDs (Installation Acceptance Test could not be located or different templates have been used
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Healthcare Inc.
Philips Healthcare Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report