Z-1490-2017 Class II Terminated
FDA device recall Z-1490-2017 was initiated by Siemens Medical Solutions USA, Inc on February 14, 2017 and is designated Class II. Reason for recall: Software update The recall status is terminated (terminated December 18, 2017). Affected quantity: 80 systems.
Recall Details
- Product Type
- Devices
- Report Date
- March 29, 2017
- Initiation Date
- February 14, 2017
- Termination Date
- December 18, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 80 systems
Product Description
ONCOR" Avant-garde
Reason for Recall
Software update
Distribution Pattern
Distributed throughout the United States
Code Information
Device Model# 1940035