FDA Adverse Event
Malfunction
Summary report: N
MICROLAB AT PLUS 2
MDR report key: 456862
·
Received April 24, 2003
Report
- Report Number
- 2915796-2003-00014
- Event Type
- Malfunction
- Date Received
- April 24, 2003
- Date of Event
- April 4, 2003
- Report Date
- April 24, 2003
- Manufacturer
- HAMILTON BONADUZ AG
- Product Code
- JTC
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TN, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
HAMILTON CO WAS INFORMED IN APRIL 2003 OF AN EVENT THAT OCCURRED IN 2003, IN WHICH THE HAMILTON MICROLAB AT +2 INSTRUMENT REPORTEDLY RAISED TUBE LIFTER B6 WHEN TUBE LIFTER C6 WAS SUPPOSED TO BE LIFTED AND DID NOT GENERATE AN ERROR MESSAGE. NO DEATH OR INJURY RESULTED FROM THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MICROLAB AT PLUS 2 | MICROTITER DILUTING/DISPENSING | JTC | HAMILTON BONADUZ AG | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |