ASSY, CNTRL UNIT, FREEDOM CYCLER (REFURB)
Report
- Report Number
- 2937457-2014-01839
- Event Type
- Injury
- Date Received
- July 24, 2014
- Date of Event
- May 16, 2014
- Report Date
- June 14, 2014
- Manufacturer
- FRESENIUS MEDICAL CARE NORTH AMERICA
- Product Code
- KPF
- PMA / PMN Number
- K791584
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER
Narratives
THE PATIENT WAS ADMITTED TO THE HOSPITAL ON (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 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, 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. 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 FAMATA. 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.
DURING A CALL TO TECHNICAL SERVICES REGARDING AN ALARM ISSUE REGARDING THE CYCLER, IT WAS INDICATED BY THE PATIENT'S MOTHER THAT THE PATIENT HAD BEEN ADMITTED TO THE HOSPITAL DUE TO AN EPISODE OF PERITONITIS. THE CLINICAL MANAGER STATED THE PATIENT WAS PREVIOUSLY ADMITTED TO THE HOSPITAL FOR PERITONITIS, WAS DISCHARGED AND IS CURRENTLY COMPLETING TREATMENTS USING THE NEW CYCLER WITHOUT ISSUE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 432959 | ASSY, CNTRL UNIT, FREEDOM CYCLER (REFURB) | KPF | FRESENIUS MEDICAL CARE NORTH AMERICA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 19 MO | Hospitalization| R | ONDANSETRON| CEFEPIME| FREEDOM CYCLER CASSETTE| AMLODIPINE| AMPHOTERICIN B| FERROUS SULFATE| EPOGEN| AMOXICILLIN| VITAMIN D| PD SOLUTIONS| FLUCONAZOLE| SODIUM CHLORIDE| SOMATROPIN| KAYEXALATE| LANSOPRAZOLE| OMEPRAZOLE |