Siemens RAPIDComm¿ Data Management System — Class III medical device recall Z-2071-2014
Terminated recall by Siemens Healthcare Diagnostics Inc, reported 2014-07-23, distributed in OR, PA. RAPIDComm¿ 5.0 Screen Layout will display incorrect test names
| Recall number | Z-2071-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Healthcare Diagnostics Inc, Norwood, MA, United States |
| Recall initiated | 2014-05-22 |
| Classified | 2014-07-17 |
| Reported by FDA | 2014-07-23 |
| Terminated | 2015-05-26 |
| Distributed | OR, PA |
| Countries outside the US | DK, GB |
| Quantity | 6 systems |
| Serial numbers | 3074, 3734, 4149, 4177, 4194, 4387 |
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 for recall
RAPIDComm¿ 5.0 Screen Layout will display incorrect test names
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2071-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.