Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands MultiDiagnost-Eleva Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MultiDiagnost-Eleva
Brand
Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands
Lot Codes / Batch Numbers
MultiDiagnost-Eleva
Products Sold
MultiDiagnost-Eleva
Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands is recalling MultiDiagnost-Eleva due to A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
Recommended Action
Per FDA guidance
Philips will send a customer notification to the existing users of the affected systems to alert them of the issue and provide actions that should be taken by the customer/user in order to prevent risks to patients. Philips will contact customers to schedule a visit to inspect the foot switch and provide an addendum to the Instructions for Use (IFU) of the system detailing the appropriate cleaning and maintenance instructions. (Philips reference 2023-IGT-BST-011).
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026