FDA Adverse Event
Death
Summary report: N
PENTIP_31GX5MM_UNF
MDR report key: 23244619
·
Received October 8, 2025
Report
- Report Number
- MW5176987
- Event Type
- Death
- Date Received
- October 8, 2025
- Report Date
- October 3, 2025
- Manufacturer
- OWEN MUMFORD, LTD.
- Product Code
- FMI
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- US
- Reporter Occupation
- PATIENT FAMILY MEMBER OR FRIEND
- Health Professional
- *
Narratives
Description of Event or Problem · 0
THE CAUSE OF DEATH WAS NOT PROVIDED BY THE REPORTER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2574627 | PENTIP_31GX5MM_UNF | NEEDLE, HYPODERMIC, SINGLE LUMEN | FMI | OWEN MUMFORD, LTD. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Female | Death |