FDA Device recall Z-1717-2014
Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems are radiographic systems used in hospitals, clinics, and medical prac…
- FDA Device
- Class II
- terminated
- Published 2014-06-11
On 2014-06-11 the FDA classified a Class II recall of Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems are radiographic systems used in hospitals, clinics, and medical prac… by Siemens Medical Solutions Usa, citing excessive usage of cleaning liquid on Siemens Ysio Systems may cause infiltration of the generator console, which may lead to a short circuit causing an unintended release of radi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1717-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-09 |
| Published | 2014-06-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems are radiographic systems used in hospitals, clinics, and medical practices. Ysio enables radiographic and tomographic exposures of 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.) ad emergency (trauma, critical ill) applications. Exposures may be taken with the patient sitting, standing, or in the prone position. The Ysio System is not meant for mammography. The Ysio uses an integrated or portable digital detector for generating diagnostic images by converting x-rays into electronic signals. Ysio is also designed to be used with conventional film/screen or Computed Radiography *CR) cassettes.
Reason
Excessive usage of cleaning liquid on Siemens Ysio Systems may cause infiltration of the generator console, which may lead to a short circuit causing an unintended release of radiation.
Identifiers
| code_info | Model nos. 10281013,10281163 with serial nos. 30080 23071 20045 31072 22523 22776 22787 31137 23021 20034…Model nos. 10281013,10281163 with serial nos. 30080 23071 20045 31072 22523 22776 22787 31137 23021 20034 20112 22775 22279 22283 22280 22875 22290 22576 22848 31060 31136 31064 31138 22326 23068 22288 22114 22714 21100 22960 23082 22169 22601 21065 21205 31017 31135 31040 21086 22972 30038 30047 23029 22538 22658 21088 21103 31120 21224 21221 21223 21085 31122 22597 22388 22391 20115 22104 22583 23097 22943 22942 22585 22781 21089 20093 20110 21066 22404 22796 22506 21031 30040 22119 22599 22844 22148 22880 21139 21006 20155 30055 30024 21114 21112 21122 31069 21185 30051 31078 30076 31012 22429 22190 31010 31011 22146 22527 22520 22126 22128 23138 31018 22836 23083 23036 22163 20089 20107 20088 20106 21052 22727 23098 22135 22737 22872 22542 22549 22551 22567 22500 31075 22449 30032 22350 31128 22389 31004 22984 30028 23020 31026 31134 21213 2224 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1717-2014%22
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