FDA Adverse Event Malfunction Summary report: N

CONNECTION SHIELD

MDR report key: 2930273 · Received January 25, 2013

Report

Report Number
1416980-2013-02015
Event Type
Malfunction
Date Received
January 25, 2013
Date of Event
January 1, 2013
Report Date
January 3, 2013
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE SAMPLE WAS RECEIVED AND EVALUATED. THE SAMPLE WAS MARKED BY THE PATIENT IN ORDER TO INDICATE WHERE THE PATIENT PERCEIVED HOLES IN THE PACKAGING. THE SAMPLE WAS HELD UP TO A LIGHT SOURCE, AND NO LIGHT PENETRATION WAS NOTED. THERE WAS NO IODINE STAINING ON THE OUTSIDE OF THE POUCHES. AN EVALUATION WAS PERFORMED IN THE (B)(4) WHEREBY IODINE WAS PLACED DIRECTLY ON THE INNER SURFACE OF THE POUCH AT THE LOCATION WHERE IT HAD BEEN INDICATED THERE WAS A HOLE. THE IODINE DID NOT PENETRATE TO THE OUTER SURFACE OF THE POUCH. THE SAMPLES WERE VISUALLY INSPECTED AND NO LIGHT PENETRATION OR HOLE WAS NOTED. THIS COMPLAINT FOR A REPORT OF A PACKAGING RELATED DEFECT WAS NOT CONFIRMED. THE ROOT CAUSE WAS UNDETERMINED. A FOLLOW-UP MDR WILL BE SUBMITTED IF ANY ADDITIONAL RELEVANT INFORMATION IS RECEIVED.

Description of Event or Problem · 1

ON (B)(6) 2013, A NURSE REPORTED THAT A PATIENT HAD REPORTED THAT WHEN HE HELD HIS CLAMSHELL UP TO A LIGHT, HE COULD SEE "SMALL LIGHT HOLES" IN THE PACKAGING. THE PATIENT REPORTED THAT THE SPONGES WERE NOT DRIED OUT. THE OCCURRENCE DATE WAS NOT REPORTED. THE SAMPLE WAS AVAILABLE AND REQUESTED FOR EVALUATION. THERE WAS NO PATIENT INVOLVEMENT; THEREFORE, NO PATIENT INJURY, MEDICAL INTERVENTION, OR ADVERSE REACTION IS ASSOCIATED WITH THE REPORTED CONDITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
36005 CONNECTION SHIELD DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - SWINFORD 12J30H12

Patients

Seq Age Sex Outcome Treatment
1