FDA Adverse Event
Other
Summary report: N
SAF-T-INTIMA IV CATHETER
MDR report key: 546898
·
Received September 29, 2004
Report
- Report Number
- 9610847-2004-00011
- Event Type
- Other
- Date Received
- September 29, 2004
- Report Date
- August 26, 2004
- Manufacturer
- BECTON DICKINSON INFUSION THERAPY SYSTEMS
- Product Code
- DQO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
SAF-T-INTIMA HAS CAUSED A NEEDLESTICK.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SAF-T-INTIMA IV CATHETER | INTRAVASCULAR CATHETERS | DQO | BECTON DICKINSON INFUSION THERAPY SYSTEMS | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |