FDA Adverse Event
Summary report: N
INFUSOMAT SPACE - US VERSION
MDR report key: 3769867
·
Received April 17, 2014
Report
- Report Number
- 2523676-2014-00123
- Date Received
- April 17, 2014
- Date of Event
- August 26, 2013
- Report Date
- March 21, 2014
- Manufacturer
- B. BRAUN MELSUNGEN AG
- Product Code
- FRN
- Product Problem
- Yes
- Report Source
- Distributor report
- Reporter Location
- MO, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
AS REPORTED BY THE USER FACILITY: TRANSFUSING BLOOD PUMP JNE 4130 REPEATEDLY ALARMING AIR. (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 236671 | INFUSOMAT SPACE - US VERSION | INFUSION PUMP | FRN | B. BRAUN MELSUNGEN AG | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |