Recall · FDA
Siemens Healthcare Diagnostics, Inc.
Siemens Healthcare Diagnostics, Inc. issued a Class II FDA recall (Z-0591-2017) initiated 2016-09-29: FlexLab Automation Modules
| Company | Siemens Healthcare Diagnostics, Inc. |
|---|---|
| Recall number | Z-0591-2017 |
| Classification | Class II |
| Status | Terminated |
| Category | Devices |
| Initiated | 2016-09-29 |
| Product | FlexLab Automation Modules |
FAQ
What did Siemens Healthcare Diagnostics, Inc. recall?
FlexLab Automation Modules