ClearanceBrief
Recall Z-1055-2019 ยท KPR System, X-Ray, Stationary

Philips North America, LLC

MultiDiagnost Eleva w/ Flat Detector, Product codes 708034, 708037, 708038 Product Usage: As a multifunctional I universal imaging application system, General RIF, Fluoroscopy, Radiography and Angiography can be performed along with more specialized interventional applications on human patients. This includes the following general areas: Digestive system: Swallowing studies, Oesophagus, Stomach

DateFeb 28, 2019
StatusTerminated
ReasonThe locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
Root causeComponent design/selection
ActionOn February 28, 2019, the firm notified customers via an Urgent Field Safety Notice letter. The letter informed customers that the affected systems would be inspected for missing locking plates. Customers were asked to place a copy of the Field Safety Notice with the documentation of the system until the system has been inspected by Philips. Philips will inspect all potentially affected systems free of charge. If a locking plate is found missing, Philips will secure the system until a locking plate is installed so that use of the system can continue. You will be contacted by your local Phili
Quantity1969
DistributionUS Nationwide domestic distribution, and worldwide international distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K050151MULTIDIAGNOST ELEVA
Philips Medical Systems North America, Inc., Feb 9, 2005