Recall Z-0590-2017— 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: Aptio Automation Modules. Reason: Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems..
- 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
Aptio Automation Modules
Reason for recall
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
Data sourced from openFDA. This site is unofficial and independent of the FDA.