Recall Z-2071-2014— Siemens Healthcare Diagnostics Inc
Class III · Terminated
Class III FDA medical device recall by Siemens Healthcare Diagnostics Inc, initiated 2014-05-22, terminated 2015-05-26. FDA's recall record names no specific 510(k) clearance for this event. 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.
- Recalling firm
- Siemens Healthcare Diagnostics Inc
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2014-05-22
- Terminated
- 2015-05-26
- Firm location
- Norwood, MA, United States
Product description
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.