FDA recall Z-1339-2020

Siemens Medical Solutions USA, Inc · Class II · device

Product

Ysio Max, model no. 10762470 - Product Usage: The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures f the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and bariatric patients. It can also be used for intravenous, small interventions (like biopsy, punctures, etc.) and emergency (trauma, critical ill) applications. Exposures may be taken with the patient sitting, standing, or in the prone position. The Ysio max system is not meant for mammography.

Reason for recall

A software bug may lead to one image to be assigned to two different patients, which could potentially affect medical diagnosis.

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-1339-2020