FDA recall record

Siemens Medical Solutions USA syngo.CT VA20A, VA30A and VA40A in: syngo.via RT Image Suite / recall — FDA Z-2446-2021

Potential for data loss when using the contouring or patient marking workflow when editing a structure set after saving and reopening a study, resulting…

Class IIclassification
Z-2446-2021official record ID
Sep 22, 2021report date

Recall record at a glance

Official recordZ-2446-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSiemens Medical Solutions USA, Inc.
Report dateSep 22, 2021
Recall initiation dateAug 16, 2021
Quantity44 systems
LocationMalvern, PA, United States

Official product description

syngo.CT VA20A, VA30A and VA40A in: syngo.via RT Image Suite / Sim&Go SOMATOM go.Now SOMATOM go.Up SOMATOM go.All SOMATOM go.Top SOMATOM go.Sim SOMATOM go.Open Pro and SOMATOM X.cite Material Numbers: 11061620 11061628 11061630 11061640 11061660 11061670

Why the product was recalled

Potential for data loss when using the contouring or patient marking workflow when editing a structure set after saving and reopening a study, resulting in an incomplete structure set sent to the treatment planning system (TPS).

Distribution information

US Nationwide 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: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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