Z-0808-2018 Class II Terminated
FDA device recall Z-0808-2018 was initiated by Siemens Medical Solutions USA, Inc on August 31, 2017 and is designated Class II. Reason for recall: 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 di… The recall status is terminated (terminated October 1, 2018). Affected quantity: 30.
Recall Details
- Product Type
- Devices
- Report Date
- March 7, 2018
- Initiation Date
- August 31, 2017
- Termination Date
- October 1, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 30
Product Description
Syngo.via systems with SW VB20A
Reason for Recall
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.
Distribution Pattern
Nationwide Distribution.
Code Information
10496180