ClearanceBrief
Recall Z-2404-2023 ยท KPR System, X-Ray, Stationary

Philips Medical Systems Nederland B.V.

MultiDiagnost-Eleva

DateSep 7, 2023 (initiated Jul 19, 2023)
StatusOpen, Classified
ReasonA foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
Root causeRadiation Control for Health and Safety Act
ActionPhilips 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).
Quantity5432 systems in total
DistributionUS Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K023441PHILIPS MULTIDIAGNOST ELEVA
Philips Medical Systems, Oct 30, 2002
K050151MULTIDIAGNOST ELEVA
Philips Medical Systems North America, Inc., Feb 9, 2005