FDA Adverse Event Malfunction Summary report: N

ACCESS

MDR report key: 2210553 · Received August 12, 2011

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

Additional Manufacturer Narrative · 1

(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.

Additional Manufacturer Narrative · 1

(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.

Description of Event or Problem · 1

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