Syngo.via systems with SW VB20A recall: Software Issue
Syngo.via systems with SW VB20A
Why was Syngo.via systems with SW VB20A recalled?
A software update was released on August 22, 2017. Performing this software installation and upgrading syngo.via system to the software version VB20A_HF02 will resolve various bugs and inconsistent diagnosis with the old system.
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?
10496180
- Product
- Syngo.via systems with SW VB20A
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 30
- Distribution
- Nationwide Distribution.
- Recall date
- March 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)