FDA recall record

Philips Electronics CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system recall — FDA Z-0330-2018

The tube adapter-plate green/yellow protective earthing (PE) wire was removed. and spacers with different thickness were used to position pre-loc ring in…

Class IIclassification
Z-0330-2018official record ID
Jan 17, 2018report date

Recall record at a glance

Official recordZ-0330-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPhilips Electronics North America Corporation
Report dateJan 17, 2018
Recall initiation dateOct 19, 2017
Quantity10
LocationAndover, MA, United States

Official product description

CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a multi-functional general R/F system. It is suitable for all routine radiography and fluoroscopy exams, including specialist areas like angiography or pediatric work, excluding mammography

Why the product was recalled

The tube adapter-plate green/yellow protective earthing (PE) wire was removed. and spacers with different thickness were used to position pre-loc ring in respect to focal spot in specified distance.

Distribution information

Worldwide Distribution - US Distribution and to the countries of : France, Germany, Luxembourg and New Zealand.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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