FDA Adverse Event
Summary report: N
BD VACUTAINER SAFETY-LOK BLOOD COLLECTION SET
MDR report key: 3973304
·
Received June 23, 2014
Report
- Report Number
- 3973304
- Date Received
- June 23, 2014
- Date of Event
- June 22, 2014
- Report Date
- June 23, 2014
- Manufacturer
- BECTON, DICKINSON AND COMPANY
- Product Code
- JKA
- Report Source
- User Facility report
- Reporter Location
- LA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
SAFETY COVER OF NEEDLE OF BLOOD COLLECTION SET WAS LOOSE IN PACKAGE AND NEEDLE WAS EXPOSED. NEEDLE COULD EASILY PIERCE THROUGH PACKAGING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 365768 | BD VACUTAINER SAFETY-LOK BLOOD COLLECTION SET | TUBES, VIALS, SYSTEMS, SERUM SEPARATORS, BLOOD COLLECTION | JKA | BECTON, DICKINSON AND COMPANY | 23G X 3/4" X 12" | 3325806 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |