FDA recall record

Siemens Medical Solutions USA Sensis Vibe Systems with Software Version VD10B, Model Numbers recall — FDA Z-2688-2017

Software error. In Sensis Vibe systems with software version VD10B, a software error can result in: problems generating a report and/ or - information…

Class IIclassification
Z-2688-2017official record ID
Jul 12, 2017report date

Recall record at a glance

Official recordZ-2688-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSiemens Medical Solutions USA, Inc.
Report dateJul 12, 2017
Recall initiation dateMay 16, 2017
QuantityUS: 13 units
LocationMalvern, PA, United States

Official product description

Sensis Vibe Systems with Software Version VD10B, Model Numbers 10765502, 10910620, 11007641, 6648161 --- Programmable diagnostic computer,

Why the product was recalled

Software error. In Sensis Vibe systems with software version VD10B, a software error can result in: problems generating a report and/ or - information from different examinations of the same patient being combined into one report. --- The error causes information from two examinations to be combined into one report. This does not result in a hazardous situation; however, if the erroneous report has been used for treatment or diagnosis, this can potentially result in an incorrect treatment or diagnosis.

Distribution information

US Distribution to the states of : IN, MI, IA

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: Letter.

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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