CE INTERMATE LV 250, 24 PACK,50126
Report
- Report Number
- 6000001-2011-01958
- Event Type
- Malfunction
- Date Received
- March 17, 2011
- Date of Event
- February 21, 2011
- Report Date
- March 2, 2011
- Manufacturer
- BAXTER HEALTHCARE - IRVINE
- Product Code
- FRN
- PMA / PMN Number
- K910425
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WY, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). ONE SAMPLE WAS RECEIVED BY BAXTER FOR EVALUATION. THE REPORTED CONDITION OF "BROKEN JUNCTION NEAR THE LUER LOCK AND BLUE WINGED CAP" WAS CONFIRMED. THIS IS A SINGLE USE DEVICE AND WILL NOT BE REPAIRED. NO OTHER OBSERVATION WAS FOUND. SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM; THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. A BATCH REVIEW WAS CONDUCTED AND NO ISSUES WERE FOUND RELATED TO THE REPORTED CONDITION DURING THE MANUFACTURE OF THE LOT.
(B)(4). ADDITIONAL NARRATIVE: THE DEVICE HAS BEEN RECEIVED BY BAXTER FOR EVALUATION; HOWEVER, THE EVALUATION HAS NOT YET BEEN COMPLETED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE EVALUATION AND/OR SHOULD ANY ADDITIONAL INFORMATION BECOME AVAILABLE.
IT WAS REPORTED TO BAXTER HEALTHCARE THAT ONE (1) CE INTERMATE LV250 DEVICE WAS DISCOVERED WITH BROKEN TUBING NEAR THE LUER LOCK/BLUE WINGED CAP JUNCTION. ACCORDING TO THE CUSTOMER, THIS WAS OBSERVED OUT OF THE PACKAGING/BEFORE USE. THIS DEVICE DOES HAVE THE BROKEN END PIECE TO EVALUATE. NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 3 OF 4 WITH THE SAME REPORTED PROBLEM FROM THIS FACILITY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CE INTERMATE LV 250, 24 PACK,50126 | PUMP, INFUSION | FRN | BAXTER HEALTHCARE - IRVINE | 10M079 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |