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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
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching...
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
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
Recall
Active
FDA
Official source
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
Recall
Active
FDA
Official source
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