ClearanceBrief
Recall Z-1000-2023 ยท OWB Interventional Fluoroscopic X-Ray System

Siemens Medical Solutions USA, Inc

AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF

DateJan 20, 2023 (initiated Dec 9, 2022)
StatusOpen, Classified
ReasonThere is potential for the footrest to detach from the patient table during use.
Root causeProcess control
ActionA Customer Safety Advisory Notification (CSAN) was distributed to affected consignees beginning December 9, 2022. The CSAN was distributed to inform the customers about a preventative measure to exclude any potential risk of patient injury caused by the footrest detaching from the patient table during examination. Together with the CSAN, an addendum to the operator manual is distributed containing additional details and illustrations on how to securely attach the footrest to further improve the understanding of handling the footrest. Refer to the CSAN with addendum and copies of the Instructio
Quantity654 units
DistributionWorldwide distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K051602AXIOM SIRESKOP SD
Siemens Medical Systems, Inc., Jul 7, 2005
K992660URF DIGITAL - OT
Siemens Medical Solutions USA, Inc., Nov 5, 1999