ClearanceBrief
Recall Z-0985-2019 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.

DateFeb 8, 2019
StatusTerminated
ReasonThe swivel arm holding the monitors may become dislodged from the carrying arm.
Root causeDevice Design
ActionThe firm, Siemens, issued an "URGENT: MEDICAL DEVICE CORRECTION "on 2/8/19 to its customers. The letter is identifying the problem, risk, actions to take and corrective action. The customers were instructed to do the following: Immediately examine your inventory and quarantine product subject to recall (if applicable). or To avoid the risk until implementation of the corrective action, it is strongly recommended not to move and position monitors above the system table. As an alternative and if clinically applicable, monitors can also be used when they are left in the parking position. In addit
Quantity191
DistributionUS Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K173639Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max, Multitom Rax
Siemens Medi Cal Solutions, Inc., Apr 2, 2018