FDA Adverse Event
Other
Summary report: N
VACUTAINER BRAND TUBE, 13X75MM, 5ML, GREEN-HEMOGARD, LIHEPAR
MDR report key: 300017
·
Received October 12, 2000
Report
- Report Number
- 1917413-2000-00023
- Event Type
- Other
- Date Received
- October 12, 2000
- Date of Event
- September 25, 2000
- Report Date
- October 12, 2000
- Manufacturer
- BECTON DICKINSON AND COMPANY
- Product Code
- JKA
- Removal / Correction Number
- NA
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
LAB. TECH. CUT FINGER WHILE OPENING A TUBE. INCIDENT HAS BEEN REPORTED TO OCCUPATIONAL MEDICINE IN FRANCE. BLOOD TESTING FOR INFECTIOUS FLUIDS HAS BEEN PERFORMED AS PER HOSP POLICY. 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 | VACUTAINER BRAND TUBE, 13X75MM, 5ML, GREEN-HEMOGARD, LIHEPAR | LITHIUM HEPARIN TUBE | JKA | BECTON DICKINSON AND COMPANY | NA | 0017035 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |