FDA Adverse Event
Malfunction
Summary report: N
RAPID INFUSER RI-2, 120V, 750 ML/MIN
MDR report key: 23108712
·
Received September 22, 2025
Report
- Report Number
- 23108712
- Event Type
- Malfunction
- Date Received
- September 22, 2025
- Date of Event
- September 3, 2025
- Report Date
- September 12, 2025
- Manufacturer
- BELMONT INSTRUMENT LLC
- Product Code
- LGZ
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- AZ
- Reporter Occupation
- RISK MANAGER
- Health Professional
- N
Narratives
Description of Event or Problem · 0
RAPID INFUSER THREW AN ERROR TO CHECK TEMPERATURE PROBES FOR BLOCKAGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2700362 | RAPID INFUSER RI-2, 120V, 750 ML/MIN | WARMER, THERMAL, INFUSION FLUID | LGZ | BELMONT INSTRUMENT LLC | 903-00039 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 38 YR | Female |