LINE SET FOR AQUARIUS
Report
- Report Number
- 1423500-2011-00781
- Event Type
- Malfunction
- Date Received
- January 19, 2011
- Date of Event
- November 25, 2010
- Report Date
- December 27, 2010
- Manufacturer
- HAEMOTRONICS SPA
- Product Code
- FJK
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- NURSE
Narratives
(B)(4). THIS COMPLAINT COULD NOT BE CONFIRMED DURING BAXTER AND HAEMOTRONIC'S SAMPLE EVALUATION. A BATCH REVIEW WAS CONDUCTED AND NO ISSUES WERE FOUND RELATED TO THE REPORTED CONDITION DURING THE MANUFACTURE OF THE LOT. BECAUSE THE COMPLAINT COULD NOT BE CONFIRMED, ROOT CAUSE COULD NOT BE DETERMINED. SIMILAR REPORTS HAVE BEEN RECEIVED BY BAXTER FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED.
(B)(4). THIS PRODUCT IS MANUFACTURED FOR DISTRIBUTION OUTSIDE OF THE UNITED STATES (US); THEREFORE, IT DOES NOT HAVE A US 510K NUMBER. HOWEVER, THIS MDR IS BEING SUBMITTED BECAUSE IT IS THE SAME AS OR SIMILAR TO A PRODUCT DISTRIBUTED WITHIN THE US. THE DEVICE HAS BEEN RECEIVED BY BAXTER, AND THE EVALUATION HAS NOT YET BEEN COMPLETED. A FOLLOW-UP MDR WILL BE SUBMITTED UPON COMPLETION OF THE EVALUATION OR IF ANY ADDITIONAL INFORMATION IS RECEIVED.
A NURSE REPORTED TO BAXTER (B)(4) THAT DURING PREFILLING A LEAK WAS NOTICED IN THE TUBING. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION REPORTED. THIS INCIDENT WAS PRIOR TO PATIENT USE AND NO PATIENT WAS CONNECTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LINE SET FOR AQUARIUS | SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE | FJK | HAEMOTRONICS SPA | B101688 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |