FDA Adverse Event Malfunction Summary report: N

LINE SET FOR AQUARIUS

MDR report key: 1964295 · Received January 19, 2011

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

Additional Manufacturer Narrative · 1

(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.

Additional Manufacturer Narrative · 1

(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.

Description of Event or Problem · 1

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