FDA Adverse Event Injury Summary report: N

LIBERTY CYCLER SET, SINGLE CONN./EXT.DL

MDR report key: 3082494 · Received April 25, 2013

Report

Report Number
8030665-2013-00233
Event Type
Injury
Date Received
April 25, 2013
Date of Event
March 25, 2013
Report Date
March 28, 2013
Manufacturer
REYNOSA MFG
Product Code
FKX
PMA / PMN Number
K043363
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

MEDICAL RECORDS WERE REQUESTED AND HAVE NOT BEEN RECEIVED BY THE MFR TO DATE. AT THE CONCLUSION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED WITH THE RESULTS OF THE CLINICAL AND PLANT INVESTIGATIONS. THIS MEDWATCH REPORT IS ASSOCIATED WITH MDR #S 8030665-2013-00234, 2937457-2013-00051, 2937457-2013-00052.

Description of Event or Problem · 1

A PERITONEAL DIALYSIS PT HAS REPORTED THAT DIALYSIS SOLUTION WAS LEAKING OUT OF THE CASSETTE AND INTO THE CYCLER DURING TREATMENT. THE PERITONEAL DIALYSIS (PD) NURSE STATED THAT THE PT CALLED HER REPORTING THAT DURING TREATMENT, PT SAW A LEAK WHEN HE OPENED THE MACHINE CYCLER SET COMPARTMENT. THERE ARE TWO OCCURRENCES: (B)(6) 2013 AND (B)(6) 2013 AND THE ORDER OF THE EVENTS IS THE SAME. ON (B)(6) 2013, THE PT DID MANUAL EXCHANGES AND NO PROBLEMS OCCURRED. ON THE MORNING OF (B)(6) 2013, THE PT WENT TO THE CLINIC WITH A CLOUDY DRAIN BAG AND THE PT WAS PLACED ON ANTIBIOTICS PROPHYLACTICALLY. RN CALLED TO GET CYCLER REPLACED AND SHE TOLD THE PT TO NOT USE THE CYCLER SETS AND THE PT HAS. IN ADDITION, SHE TOLD THE PT TO KEEP THE SAMPLES. UPON F/U ON (B)(6) 2013, PT STATED THAT HE WAS DIAGNOSED WITH PERITONITIS. PT TOOK ANTIBIOTICS FOR 2 WEEKS AND NOW HIS EFFLUENT IS CLEAR, THE PT IS FINE, THE PERITONITIS HAS RESOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
178599 LIBERTY CYCLER SET, SINGLE CONN./EXT.DL LIBERTY DIALYSIS CYCLER TUBING FKX REYNOSA MFG

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention LIBERTY DIALYSIS CYCLER