Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by Philips Healthcare Inc. Due to An inspection of IATD (Installation Acceptance Test Document)IA...
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. Catalog Numbers: 704031, 704032, 704035, 704060, 704062 This system is used for making x-ray exposures for diagnostics
Quantity: 116 units
Why Was This Recalled?
An inspection of IATD (Installation Acceptance Test Document)IA SID (Source Image Distance) records shows table height measurements out of specification with the consequence of potential system mis-alignment
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