Manufacturer
79 recalls in our database name Philips Medical Systems Nederlands as the manufacturing or recalling firm.
Of the 79 recalls from Philips Medical Systems Nederlands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 30 (38%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Certain low-voltage power supplies in Philips Allura Xper interventional X-ray systems may fail, potentially causing loss of imaging functionality. 42 devices are affected worldwide.
Philips is recalling 229 Azurion Interventional Fluoroscopic X-ray Systems because a software defect may cause radiation levels too low for diagnostic images.
Philips is recalling four Ingenia Ambition MR systems because the Magnet Energization Device may have residual voltage, posing an electrical shock risk to personnel.
Philips Medical Systems is recalling 7,209 foot switches used with Allura Xper systems because pedals may bend, causing an inability to make live fluoroscopy images or exposures.
Philips Medical Systems is recalling 7,209 foot switches used with specific imaging systems because bent pedals may prevent live fluoroscopy images or exposures.
Philips is recalling 11,226 Intera IT MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Ingenia Elition S MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling Intera Achieva 1.5T Nova MRI systems because ceiling speakers may be pulled by the magnetic field and fall.
Philips is recalling Ingenia 1.5T S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Panorama 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Multiva MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Achieva XR MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Ingenia Elition X MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Ingenia 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Ingenia 1.5T CX MRI systems because ceiling speakers may be pulled by the magnetic field and fall.
Philips is recalling 11,226 Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling MR RT MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.