FDA Adverse Event
Other
Summary report: N
SST BRAND TUBE - 16X100MM, 8.3ML, RED/GRAY CONVENTIONAL-GLAS
MDR report key: 289715
·
Received August 11, 2000
Report
- Report Number
- 1024879-2000-00019
- Event Type
- Other
- Date Received
- August 11, 2000
- Date of Event
- June 20, 2000
- Report Date
- August 9, 2000
- Manufacturer
- BECTON DICKINSON AND CO
- Product Code
- JKA
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
TUBES BROKE IN CENTRIFUGE. WHILE REMOVING BROKEN GLASS FROM CENTRIFUGE, TECHNICIAN CUT A HAND. ANOTHER TECHNICIAN RECEIVED ANOTHER CUT TO THE FINGER WHEN ANOTHER TUBE BROKE IN THE HAND. BOTH TECHNICIANS WERE SEEN BY INFECTIOUS CONTROL. BOTH HAD BASELINE TESTING FOR HUMAN IMMUNODEFICIENCY VIRUS AND HEPATITIS B VIRUS. BODY FLUID WAS NOT INFECTIOUS. IT WAS CALCULATED THAT THE SPEED OF CENTRIFUGE EXCEEDED RECOMMENDED SPEED. ACCOUNT WAS NOTIFIED AND INFORMED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SST BRAND TUBE - 16X100MM, 8.3ML, RED/GRAY CONVENTIONAL-GLAS | SST BRAND TUBE | JKA | BECTON DICKINSON AND CO | NA | 0D914 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |