FDA Adverse Event
Other
Summary report: N
SST BRAND TUBE - 16X125MM, 13ML, RED/GRAY-CONVENTIONAL TUBE
MDR report key: 297236
·
Received September 21, 2000
Report
- Report Number
- 1024879-2000-00022
- Event Type
- Other
- Date Received
- September 21, 2000
- Report Date
- September 21, 2000
- Manufacturer
- BECTON DICKINSON AND CO.
- Product Code
- JKA
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
- Reporter Location
- NC, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
WHILE UNCAPPING TUBES, 2 TECHNOLOGISTS ON 2 SEPARATE OCCASSIONS WERE INJURED. BOTH RECEIVED CUTS ON THEIR FINGERS. BOTH TECHNOLOGISTS WERE SEEN IN THE EMERGENCY ROOM AND RECEIVED BASELINE TESTING FOR HIV AND HEPATITIS. REVIEW OF THE DATABASE INDICATES NO OTHER ISSUES WITH REGARDS TO THIS PRODUCTION LOT NUMBER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SST BRAND TUBE - 16X125MM, 13ML, RED/GRAY-CONVENTIONAL TUBE | SST TUBE | JKA | BECTON DICKINSON AND CO. | NA | 9F923 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |