FDA Adverse Event
Malfunction
Summary report: N
BECTON DICKINSON & COMPANY
MDR report key: 20993363
·
Received December 20, 2024
Report
- Report Number
- 3014527682-2024-00024
- Event Type
- Malfunction
- Date Received
- December 20, 2024
- Report Date
- December 20, 2024
- Manufacturer
- BECTON DICKINSON AND COMPANY
- Product Code
- FMF
- PMA / PMN Number
- K980987
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- NURSE
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
THE CUSTOMER REPORTED THE FOLLOWING: THERE WERE TWO INCIDENTS INVOLVING A SYRINGE THAT BROKE IN THE MIDDLE OF SURGERY AND TWO SEPARATE PHYSICIANS GOT STUCK WITH NEEDLES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2374666 | BECTON DICKINSON & COMPANY | 10 ML NON-STERILE LUER-LOK TIP | FMF | BECTON DICKINSON AND COMPANY | 301029 | 4046619 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |