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Philips North America Llc alerts
Verified recalls, refunds, lawsuits, and settlements involving Philips North America Llc.
Recall
Active
FDA
Official source
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment. Product...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment. Product...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker...
- Company
- Philips North America Llc
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration