CE INTERMATE LV 100, 24 PACK,50126
Report
- Report Number
- 6000001-2010-04150
- Event Type
- Malfunction
- Date Received
- October 18, 2010
- Date of Event
- September 9, 2010
- Report Date
- September 16, 2010
- Manufacturer
- BAXTER HEALTHCARE - IRVINE
- Product Code
- FRN
- PMA / PMN Number
- K910425
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). DEVICE EVALUATION: ONE UNIT WAS RECEIVED BY BAXTER FOR EVALUATION. VISUAL EXAMINATION OF THE UNIT CONFIRMED THE DISTAL END LUER LOCK TO BE BROKEN. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. A BATCH REVIEW WAS CONDUCTED AND REVEALED THAT THE PRODUCT MET ALL ACCEPTANCE CRITERIA FOR RELEASE. THIS IS A SINGLE USE DEVICE AND WILL NOT BE REPAIRED.
(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 THAT THE TUBING OF ONE (1) CE INTERMATE LV100 DEVICE WAS DISCOVERED BROKEN OFF AT THE JUNCTION OF THE LUER LOCK AND BLUE WINGED CAP. THIS OCCURRED DURING FILLING WITH NORMAL SALINE. THERE HAS BEEN NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 2 OF 5 WITH THE SAME REPORTED PROBLEM FROM THIS FACILITY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CE INTERMATE LV 100, 24 PACK,50126 | PUMP, INFUSION | FRN | BAXTER HEALTHCARE - IRVINE | 10A002 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |