FDA recall record

Siemens Medical Solutions USA YSIO X.Pree recall — FDA Z-0730-2022

For the automated multi-image-acquisition procedure Ortho x-ray collimation is set in a preparative stage for the entire examination area prior to the…

Class IIclassification
Z-0730-2022official record ID
Apr 13, 2022report date

Recall record at a glance

Official recordZ-0730-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSiemens Medical Solutions USA, Inc.
Report dateApr 13, 2022
Recall initiation dateMar 7, 2022
Quantity53 units
LocationMalvern, PA, United States

Official product description

YSIO X.Pree

Why the product was recalled

For the automated multi-image-acquisition procedure Ortho x-ray collimation is set in a preparative stage for the entire examination area prior to the exam. During acquisition of each individual x-ray image, the x-ray collimator is automatically positioned in a way that the subsequent series of acquisition covers the defined field of view needed for each step. However, during the acquisition the collimation area displayed to the operator on the User Interface does not correctly represent the collimation area specified by the system. It indicates to the user an open collimator instead, e.g., the information displayed on the User Interface shows wider area of collimation than values preset prior to the examination. However, the collimation of the x-ray is performed correctly and always matches the examination area predefined by the user.

Distribution information

US Nationwide, Worldwide distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: FDA Mandated. Initial notification: Letter.

What to do next

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About this record

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