FDA Adverse Event
Malfunction
Summary report: N
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
MDR report key: 1233030
·
Received November 18, 2008
Report
- Report Number
- 6000001-2007-05711
- Event Type
- Malfunction
- Date Received
- November 18, 2008
- Date of Event
- April 6, 2007
- Report Date
- April 6, 2007
- Manufacturer
- BAXTER HEALTHCARE PTE.LTD.
- Product Code
- FRN
- Removal / Correction Number
- 2005-019-MD
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
EVALUATION SUMMARY: DURING PRODUCT EVALUATION, AIR IN LINE PRINTED CIRCUIT BOARD (AIL PCB) NEEDS CALIBRATION WAS OBSERVED. FAILURE CODE 810:04 IN THE EVENT HISTORY CONFIRMS THE AIL PCB NEEDS CALIBRATION. THIS FAILURE CODE IS MANIFESTED AS A RESULT OF THE AIL PCB BEING DEFECTIVE. THE AIL PCB ON CHANNEL A WAS RECALIBRATED.
Description of Event or Problem · 1
THE DEVICE WAS RETURNED TO BAXTER FOR SERVICE. DURING TESTING, THE BAXTER TECHNICIAN REPORTED AN INFUSION PUMP WITH A AIR IN LINE PRINTED CIRCUIT BOARD (AIL PCB) NEEDS CALIBRATION. ACCORDING TO THE HOSPITAL REPRESENTATIVE, NO PATIENT INJURY OR MEDICAL INTERVENTION HAS BEEN REPORTED RELATED TO THIS DEVICE. NO ADDITIONAL INFORMATION IS KNOWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP | INFUSION PUMP | FRN | BAXTER HEALTHCARE PTE.LTD. | N/A | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |