FDA Adverse Event
Other
Summary report: N
250E NDL 25 X 5/8 A
MDR report key: 480010
·
Received August 22, 2003
Report
- Report Number
- 1017768-2003-00008
- Event Type
- Other
- Date Received
- August 22, 2003
- Report Date
- May 15, 2003
- Manufacturer
- THE KENDALL CO
- Product Code
- FMF
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
IT WAS REPORTED TO KENDALL ON 5/15/01 THAT THE VETERIANARIAN'S FAMILY MEMBER, WHO WORKS FOR THEM, EXPERIENCED 2 CLEAN NEEDLESTICKS DUE TO BENT NEEDLES STICKING THROUGH SHEATH, WHILE THEY WERE TAKING THEM OUT OF THE BOX. LOT NUMBER GIVEN. NO SAMPLES AVAILABLE. NO SERIOUS INJURY REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 250E NDL 25 X 5/8 A | MONOJECT NEEDLE | FMF | THE KENDALL CO | * | 295829 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |