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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. alerts

Verified recalls, refunds, lawsuits, and settlements involving PHILIPS MEDICAL SYSTEMS NEDERLAND B.V..

Recall Active FDA Official source

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Azurion system; System Code Description (Model Numbers): Azurion 3 M12...

It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may,...

Company: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

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Recall Active FDA Official source

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Philips Azurion systems not configured with an optional auxiliary pan...

Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control...

Company: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

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Recall Active FDA Official source

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Integris-Allura system; System Code Description (Model Numbers):...

The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may...

Company: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Deadline: No deadline listed
Source: U.S. Food and Drug Administration

View affected products Official source