FDA recall Z-1333-2020

Siemens Medical Solutions USA, Inc · Class II · device

Product

Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological therapeutic applications such as examinations and small interventions of the urogenital tract.

Reason for recall

Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in collision control creating risk of collision with obstacles or persons when the operator uses the override function.

Distribution

US Nationwide distribution.

Key facts

Status
Terminated
Initiation date
2020-01-08
Report date
2020-02-26
Termination date
2022-06-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Malvern, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1333-2020