FDA Device recall Z-0590-2017
Aptio Automation Modules
- FDA Device
- Class II
- terminated
- Published 2016-11-23
On 2016-11-23 the FDA classified a Class II recall of Aptio Automation Modules by Siemens Healthcare Diagnostics, citing possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0590-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-09-29 |
| Published | 2016-11-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Healthcare Diagnostics |
| Distribution | US |
Product
Aptio Automation Modules
Reason
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
Identifiers
| code_info | "Refrigerated Storage Module (RSM): 10703049, 10715227, 10703036, 10713762, 10713767; "Centrifuge Module (CM): 1070303…"Refrigerated Storage Module (RSM): 10703049, 10715227, 10703036, 10713762, 10713767; "Centrifuge Module (CM): 10703032, 10713761, 10713764; "i2000SR Interface Module (i2000SR): 10989303, 10989304. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0590-2017%22
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