FDA Adverse Event
Malfunction
Summary report: N
MEDICORE
MDR report key: 24303848
·
Received February 10, 2026
Report
- Report Number
- 24303848
- Event Type
- Malfunction
- Date Received
- February 10, 2026
- Date of Event
- December 26, 2025
- Report Date
- January 29, 2026
- Manufacturer
- REGISTRAR CORP.
- Product Code
- FMK
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- RI
- Reporter Occupation
- 501
Narratives
Description of Event or Problem · 0
NO HARM TO PATIENT. THE GREEN LANCETS IN LOT L0+240929R. THEY DONT UNCAP WITHOUT HINDERING THE ABILITY TO PRICK A PATIENT.
Description of Event or Problem · 0
NO HARM TO PATIENT. THE GREEN LANCETS IN LOT L0+240929R. THEY DONT UNCAP WITHOUT HINDERING THE ABILITY TO PRICK A PATIENT.
Description of Event or Problem · 0
NO HARM TO PATIENT. THE GREEN LANCETS IN LOT L0+240929R. THEY DONT UNCAP WITHOUT HINDERING THE ABILITY TO PRICK A PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 362834 | MEDICORE | SINGLE USE ONLY BLOOD LANCET WITH INTEGRAL SHARPS INJURY PREVENTION FEATURE | FMK | REGISTRAR CORP. | L0+240929R |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Other |