FDA Adverse Event
Other
Summary report: N
ABBOTT AXSYM SYSTEM
MDR report key: 285311
·
Received July 10, 2000
Report
- Report Number
- 1628664-2000-00046
- Event Type
- Other
- Date Received
- July 10, 2000
- Date of Event
- June 7, 2000
- Report Date
- July 5, 2000
- Manufacturer
- ABBOTT MANUFACTURING, INC
- Product Code
- JJE
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MI, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
WHILE DEMONSTRATING AN AXSYM COMPONENT TO A CUSTOMER, AN ABBOTT EMPLOYEE CAUGHT THEIR FINGER IN THE SYRINGE ASSEMBLY. THE EMPLOYEE HAS AN OPEN FRACTURE OF THE LEFT FIFTH DIGIT WITH A LACERATED NAIL BED. THE EMPLOYEE REC'D SIX STITCHES AND THE HAND/FINGER IS IN A SPLINT. ADDITIONALLY, THE EMPLOYEE REC'D A TETANUS SHOT, ANTIBIOTIC AND PAIN MEDICINE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ABBOTT AXSYM SYSTEM | AUTOMATED IMMUNOASSAY ANALYZER | JJE | ABBOTT MANUFACTURING, INC | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Other |