Recall · FDA
Siemens Healthcare Diagnostics, Inc.
Siemens Healthcare Diagnostics, Inc. issued a Class II FDA recall (Z-0209-2019) initiated 2018-08-14: APTIO INPUT/OUTPUT MODULE
| Company | Siemens Healthcare Diagnostics, Inc. |
|---|---|
| Recall number | Z-0209-2019 |
| Classification | Class II |
| Status | Terminated |
| Category | Devices |
| Initiated | 2018-08-14 |
| Product | APTIO INPUT/OUTPUT MODULE |
| Reason | The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality. |
FAQ
What did Siemens Healthcare Diagnostics, Inc. recall?
APTIO INPUT/OUTPUT MODULE
Why was Siemens Healthcare Diagnostics, Inc.'s product recalled?
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.