FDA Device recall Z-2071-2014
Siemens RAPIDComm¿ Data Management System
- FDA Device
- Class III
- terminated
- Published 2014-07-23
On 2014-07-23 the FDA classified a Class III recall of Siemens RAPIDComm¿ Data Management System by Siemens Healthcare Diagnostics, citing RAPIDComm¿ 5.0 Screen Layout will display incorrect test names.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2071-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-05-22 |
| Published | 2014-07-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Healthcare Diagnostics |
| Distribution | OR, PA |
Product
Siemens RAPIDComm¿ Data Management System. The RAPIDComm¿ Data Management System manages the process of sending and receiving data from Siemens POC devices and hospital systems located in the hospital network,
Reason
RAPIDComm¿ 5.0 Screen Layout will display incorrect test names
Identifiers
| code_info | Serial Numbers: 4387, 3734, 4177, 4149, 3074, 4194 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2071-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.