Recall Z-0591-2017— Siemens Healthcare Diagnostics, Inc.
Class II · Terminated
Class II FDA medical device recall by Siemens Healthcare Diagnostics, Inc., initiated 2016-09-29, terminated 2018-09-19. FDA's recall record names no specific 510(k) clearance for this event. Product: FlexLab Automation Modules.
- Recalling firm
- Siemens Healthcare Diagnostics, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-09-29
- Terminated
- 2018-09-19
- Firm location
- Newark, DE, United States
Product description
FlexLab Automation Modules
Data sourced from openFDA. This site is unofficial and independent of the FDA.