FDA Adverse Event
Malfunction
Summary report: N
NEOMED ORAL/ENTERAL SYRINGE
MDR report key: 24250900
·
Received February 3, 2026
Report
- Report Number
- MW5183273
- Event Type
- Malfunction
- Date Received
- February 3, 2026
- Date of Event
- January 28, 2026
- Report Date
- January 29, 2026
- Manufacturer
- NEOMED, INC./AVANOS MEDICAL, INC.
- Product Code
- PNR
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- RISK MANAGER
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
SEVERAL NEOMED ORAL/ENTERAL SYRINGE 60 ML W/ENFIT CONNECTORS HAD CAPS THAT WOULD NOT STAY IN PLACE WHEN CONNECTING THEM.
Description of Event or Problem · 0
ADDITIONAL INFORMATION WAS RECEIVED ON 03/02/2026 FOR REPORT MW5183283 TO UPDATE COMMON DEVICE NAME, PROCODE AND DEVICE MANUFACTURER. PROCODE: PNR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 304254 | NEOMED ORAL/ENTERAL SYRINGE | ENTERAL SYRINGES WITH ENTERAL SPECIFIC CONNECTORS | PNR | NEOMED, INC./AVANOS MEDICAL, INC. | TY250716 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |