ACCESS
Report
- Report Number
- 6000001-2011-18690
- Event Type
- Malfunction
- Date Received
- August 12, 2011
- Date of Event
- July 1, 2011
- Report Date
- July 22, 2011
- Manufacturer
- BAXTER HEALTHCARE
- Product Code
- FPA
- PMA / PMN Number
- K962581
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
(B)(4). A SAMPLE IS NOT AVAILABLE FOR EVALUATION; THEREFORE, THE CONDITION CANNOT BE CONFIRMED OR DUPLICATED AND THE ASSIGNABLE ROOT CAUSE COULD NOT BE DETERMINED. IF ADDITIONAL INFORMATION OR SAMPLES BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED.
(B)(4). A BATCH REVIEW WAS CONDUCTED AND THERE WERE NO DEVIATIONS FOUND RELATED TO THIS REPORTED CONDITION DURING THE MANUFACTURE OF THIS LOT. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.
A CUSTOMER REPORTED TO BAXTER PRODUCT SURVEILLANCE OF A CLEAR LINK SET IN WHICH AN UNKNOWN BREAKAGE OCCURRED AT AN UNKNOWN POSITION OF A STOPCOCK AND/OR TUBING. THE SPECIFIC CONDITION AND SPECIFIC ALLEGED DEFECT WERE UNCLEAR SINCE THE CUSTOMER DID NOT HAVE THAT MUCH CLINICAL KNOWLEDGE OF THE DEVICE. THERE WAS NO PATIENT INVOLVEMENT OR MEDICAL INTERVENTION REPORTED. THE SAMPLE IS CONTAMINATED WITH BLOOD. NO ADDITIONAL INFORMATION IS AVAILABLE. THIS IS REPORT 2 OF 2 OF THE SAME REPORTED PROBLEM FROM THIS FACILITY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACCESS | SET, ADMINISTRATION, INTRAVASCULAR | FPA | BAXTER HEALTHCARE | R11B25166 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |