ClearanceBrief
Recall Z-1489-2020 ยท IZI System, X-Ray, Angiographic

Philips North America, LLC

MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038

DateDec 30, 2019
StatusTerminated
ReasonA capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
Root causeComponent design/selection
ActionOn December 30, 2019, the firm notified customers via Medical Device Correction letter. Customers were informed of the product issue and advised to do the following: If the capacitor of the Velara X-Ray fails as described (capacitor failure after large number of surges in a short period of time), please switch off the system, take it out of service immediately, and contact your local Philips representative. The firm will be resolving the issue by replacing a Printed Circuit Board (PCB) in the convertor, which prevents the capacitor from failing. PCB replacements started in January 2020. Cust
Quantity534
DistributionNationwide domestic distribution. Foreign distribution worldwide.
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