Philips SmartPath dStream MRE Recall
Philips SmartPath to dStream 3.0T MR Elastography systems can produce incorrect stiffness measurements when certain image settings are used together. This may …
Philips North America
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recalls (2026)
Every recall we are tracking for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., newest first, sourced from the FDA. If you are wondering whether your PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recall posts.
3 recalls · updated Apr 14, 2026
Philips Azurion R3.1 Software Recall
Philips Azurion systems running Software Version R3.1 have two software issues that can cause loss of X-ray imaging, loss of motorized movement, or incorrect …
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips SmartPath dStream 3.0T MRI Recall
Philips SmartPath to dStream 3.0T MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when exporting MR Elastography maps …
Philips North America
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