FDA Adverse Event
Other
Summary report: N
VACUTAINER BRAND CITRATE TUBE
MDR report key: 274285
·
Received April 17, 2000
Report
- Report Number
- 1917413-2000-00011
- Event Type
- Other
- Date Received
- April 17, 2000
- Date of Event
- April 6, 2000
- Report Date
- April 17, 2000
- Manufacturer
- BECTON DICKINSON AND COMPANY
- Product Code
- JKA
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
ONE TECH WAS INJURED WHEN REMOVING STOPPER FROM A TUBE OF BLOOD AND INJURED INDEX FINGER. FIRST AID AND BLOOD TESTING PERFORMED. SOURCE OF BLOOD WAS NON-INFECTIOUS. NO MEDICAL INTERVENTION REQUIRED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VACUTAINER BRAND CITRATE TUBE | CITRATE TUBE | JKA | BECTON DICKINSON AND COMPANY | NA | 9A851 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |