ASSY, CBTRK YBUTM FREEDOM CYCLER (REFURB)

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2014-07-24 for ASSY, CBTRK YBUTM FREEDOM CYCLER (REFURB) manufactured by Fresenius Medical Care North America.

Event Text Entries

[20974990] The following was based on medical records provided by the patient's treatment facility. The patient was hospitalized on (b)(6) 2014 through (b)(6) 2014 due to bacterial and fungal peritonitis. The patient was treated with a 14 day course of cefepime and fluconazole ip.
Patient Sequence No: 1, Text Type: D, B5


[21299936] The patient was admitted to the hospital on (b)(6) 2014 through (b)(6) 2014 after his mother reported a one day history of cloudy, purulent effluent peritoneal dialysis (pd) fluid. The patient was hospitalized on (b)(6) 2014 through (b)(6) 2014 due to bacterial and fungal peritonitis. During this time, he completed a 14 day course of cefepime and fluconazole intra-peritoneally (ip) through his dialysate. On (b)(6) 2014 his effluent pd fluid cultures were positive for enterobacter cloacae and klebsiella pneumoniae. On (b)(6) 2014 and (b)(6) 2014, pd fluid cultures were positive. The following was based on medical records provided by the patient's treatment facility. He completed a 14 day course of cefepime and fluconazole intra-peritoneally (ip) through his dialysate. On (b)(6) 2014 his effluent pd fluid cultures were positive for enterobacter cloacae and klebsiella pneumoniae. On (b)(6)2014 and (b)(6) 2014, pd fluid cultures were positive. The following was based on medical records provided by the patient's treatment facility. He completed a 14 day course of cefepime and fluconazole intraperitoneally (ip). The patient has a history of emesis which has worsened recently as well as baseline loose and frequent stools. The patient was negative for fever and chills. The patient's abdomen was non-tender with no rebound tenderness or guarding. There were normal bowel sounds. His gastrostomy tube site was clean and dry and his pd catheter showed no signs of inflammation. The patient received his last dose of fluconazole in his pd fluid on (b)(6) 2014 and did not start his fluconazole via his gastrostomy tube until (b)(6) 2014. The patient's last positive fungal culture in the pd fluid was on (b)(6) 2014 growing candida fumata. His last positive bacterial culture of the pd fluid was on (b)(6) 2014. A supplemental report will be submitted upon completion of the plant's investigation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2937457-2014-01838
MDR Report Key4016926
Report Source05,06
Date Received2014-07-24
Date of Report2014-04-24
Date of Event2014-04-20
Date Mfgr Received2014-07-18
Device Manufacturer Date2000-05-01
Date Added to Maude2014-08-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactTANYA TAFT, RN CNOR
Manufacturer Street920 WINTER ST.
Manufacturer CityWALTHAM MA 024511457
Manufacturer CountryUS
Manufacturer Postal024511457
Manufacturer Phone7816999000
Manufacturer G1FRESENIUS MEDICAL CARE NORTH AMERICA
Manufacturer Street4040 NELSON AVE.
Manufacturer CityCONCORD CA 94520
Manufacturer CountryUS
Manufacturer Postal Code94520
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameASSY, CBTRK YBUTM FREEDOM CYCLER (REFURB)
Product CodeKPF
Date Received2014-07-24
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerFRESENIUS MEDICAL CARE NORTH AMERICA
Manufacturer AddressCONCORD CA US


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2014-07-24

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