FDAClass IIFebruary 14, 2018

Syngo.plaza systems with SW VB20A recall

Syngo.plaza systems with SW VB20A, Model Number - 10863171, 10863172, 10863173 Product Usage: Syngo.plaza is a Picture Archiving and Communication…

Why was Syngo.plaza systems with SW VB20A recalled?

When a prior study is being replaced in the workflow step, in certain scenarios (based on the Display Protocol configuration) the prior study will only be replaced in the active Workflow Step and not show in all other workflow steps. The other workflow steps will continue to show the initially loaded study.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model Number - 10863171, 10863172, 10863173

Product
Syngo.plaza systems with SW VB20A, Model Number - 10863171, 10863172, 10863173 Product Usage: Syngo.plaza is a Picture Archiving and Communication…
Recalling firm
Siemens Medical Solutions USA, Inc
Quantity
76
Distribution
US Nationwide Distribution
Recall date
February 14, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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