FDA Adverse Event Malfunction Summary report: N

FOLEY CATHETER, 400 SERIES 14 FR (+/-0.1C)

MDR report key: 19927889 · Received August 7, 2024

Report

Report Number
2320762-2022-00005
Event Type
Malfunction
Date Received
August 7, 2024
Date of Event
July 28, 2022
Report Date
November 25, 2024
Manufacturer
DEROYAL INDUSTRIES, INC.
Product Code
EYC
UDI-DI
50749756596652
PMA / PMN Number
K200757
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NL
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

A USER FACILITY COMPLAINT WAS RECEIVED ON 07/28/2022 REPORTING "IN THE PAST FEW WEEKS, I HAD 2 PATIENTS WITH A RETENTION BLADDER (1X 800CC). ALL 2 OF THESE PATIENTS CAME FROM THE OR AND HAD BEEN IN THE WARD FOR SEVERAL HOURS. BECAUSE THE URINE PRODUCTION PER HOUR WAS LOW, THEY WERE BOTH FILLED SEVERAL TIMES. IN THE LATE SHIFT I FOUND OUT THAT THE BLADDER WAS FULL. WHEN RINSING, THE LIQUID GOES IN EASILY BUT DOES NOT COME OUT. PATIENTS OFTEN INDICATE THAT THEY HAVE THE FEELING THAT THEY HAVE TO AND CLEARLY HAVE A HARDER TIME. WHEN ASKING AROUND, MORE COLLEAGUES NOTICED THIS. I WAS ABLE TO SOLVE IT EVERY TIME BY EMPTYING THE BALLOON AND MOVING IT FURTHER. PREVIOUSLY WE DID 10CC IN THE DECORATION BUT NOWADAYS THERE IS MAX 5CC IN IT, MAYBE THIS IS THE PROBLEM? I HAVE AN AWAKE PATIENT THIS NIGHT WHO HAS THE SENSATION OF A FULL BLADDER AND LESS URINATION (NO RETENTION BLADDER YET). I HAVE NOW ALSO EMPTIED THE BALLOON AND PUSHED THE CATHETER ON, LATER THE PROBLEM HAS BEEN SOLVED, BUT THAT'S WHY I'M GOING TO DIM IT NOW' AFTER ASKING AROUND AT THE OTHER IC'S IN ONE HALF-DAY (WE HAVE 3) WE COME TO TELL THE NEXT ONE; · 3 COLLEAGUE CASE HISTORIES WHERE THE PATIENT HAD ENCOUNTERED RETENTION BLADDER WITH DEROYAL'S URINARY CATHETER. · 4 URINARY CATHETERS THAT LEAK URINE. · 3 TIMES IN A SHORT TIME THAT THE URINARY CATHETER WAS IN BED WITH THE PATIENT FOR NO APPARENT REASON." THIS REPORT CAME IN AS ONE COMPLAINT, BUT BECAUSE IT DESCRIBED TEN SEPARATE EVENTS, IT WILL BE REPORTED FOR EACH EVENT. THIS REPORT IS FIVE OF TEN (5/10). A SUPPLIER CORRECTIVE ACTION REQUEST (SCAR) WAS ISSUED TO THE FOLEY CATHETER SUPPLIER XERIDIEM MEDICAL DEVICES. THE SAMPLE IS NOT AVAILABLE FOR RETURN TO DEROYAL FOR EVALUATION. THIS INVESTIGATION IS NOT COMPLETE AT THIS TIME. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. WE WILL PROVIDE FOLLOW-UP REPORT ONCE MORE INFORMATION IS CONCLUDED FROM THE INVESTIGATION AND CORRECTIVE ACTIONS ARE DETERMINED.

Additional Manufacturer Narrative · 0

A SUPPLIER CORRECTIVE ACTION REQUEST (SCAR) WAS ISSUED TO THE FOLEY CATHETER SUPPLIER (XERIDIEM). ROOT CAUSE: WAS DETERMINED TO BE UNKNOWN BY THE SUPPLIER XERIDIEM AS NO EVIDENCE WAS FOUND WITH THE SUBJECT LOT OR HISTORICALLY TO SUGGEST MANUFACTURING WAS THE CAUSE OF THE REPORTED FAILURE MODE. THE DEVICE HISTORY RECORD WAS REVIEWED BY SUPPLIER XERIDIEM AND NO OBSERVATIONS DURING THE REVIEW THAT CONTRIBUTE TO THE NOTED COMPLAINT. THE COMPLAINT RECORDS WERE ALSO REVIEWED BY XERIDIEM. FOR THE PREVIOUS YEAR, THERE HAD BEEN 2 REPORTED COMPLAINTS FOR PLUGGED DRAIN LUMEN, BUT NOTHING ON DEVICE FALL OUT OR BALLOON LEAK/DEFLATE. THE SPECIFIC DEVICE WAS ALSO CONSIDERED AND NO REPORTED COMPLAINTS DOCUMENTS FOR ALL THREE FAILURE MODES. XERIDIEM STATED THAT FOR CORRECTIVE ACTION THEY WILL CONTINUE TO MONITOR FOR TRENDS. THIS INVESTIGATION IS COMPLETE AT THIS TIME. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. WE WILL PROVIDE FOLLOW-UP REPORT IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

Additional Manufacturer Narrative · 0

A USER FACILITY COMPLAINT WAS RECEIVED ON 07/28/2022 REPORTING "IN THE PAST FEW WEEKS, I HAD 2 PATIENTS WITH A RETENTION BLADDER (1X 800CC). ALL 2 OF THESE PATIENTS CAME FROM THE OR AND HAD BEEN IN THE WARD FOR SEVERAL HOURS. BECAUSE THE URINE PRODUCTION PER HOUR WAS LOW, THEY WERE BOTH FILLED SEVERAL TIMES. IN THE LATE SHIFT I FOUND OUT THAT THE BLADDER WAS FULL. WHEN RINSING, THE LIQUID GOES IN EASILY BUT DOES NOT COME OUT. PATIENTS OFTEN INDICATE THAT THEY HAVE THE FEELING THAT THEY HAVE TO AND CLEARLY HAVE A HARDER TIME. WHEN ASKING AROUND, MORE COLLEAGUES NOTICED THIS. I WAS ABLE TO SOLVE IT EVERY TIME BY EMPTYING THE BALLOON AND MOVING IT FURTHER. PREVIOUSLY WE DID 10CC IN THE DECORATION BUT NOWADAYS THERE IS MAX 5CC IN IT, MAYBE THIS IS THE PROBLEM? I HAVE AN AWAKE PATIENT THIS NIGHT WHO HAS THE SENSATION OF A FULL BLADDER AND LESS URINATION (NO RETENTION BLADDER YET). I HAVE NOW ALSO EMPTIED THE BALLOON AND PUSHED THE CATHETER ON, LATER THE PROBLEM HAS BEEN SOLVED, BUT THAT'S WHY I'M GOING TO DIM IT NOW' AFTER ASKING AROUND AT THE OTHER IC'S IN ONE HALF-DAY (WE HAVE 3) WE COME TO TELL THE NEXT ONE: 3 COLLEAGUE CASE HISTORIES WHERE THE PATIENT HAD ENCOUNTERED RETENTION BLADDER WITH DEROYAL'S URINARY CATHETER. 4 URINARY CATHETERS THAT LEAK URINE. 3 TIMES IN A SHORT TIME THAT THE URINARY CATHETER WAS IN BED WITH THE PATIENT FOR NO APPARENT REASON." THIS REPORT CAME IN AS ONE COMPLAINT, BUT BECAUSE IT DESCRIBED TEN SEPARATE EVENTS, IT WILL BE REPORTED FOR EACH EVENT. THIS REPORT IS FIVE OF TEN (5/10). A SUPPLIER CORRECTIVE ACTION REQUEST (SCAR) WAS ISSUED TO THE FOLEY CATHETER SUPPLIER XERIDIEM MEDICAL DEVICES. THE SAMPLE IS NOT AVAILABLE FOR RETURN TO DEROYAL FOR EVALUATION. THIS INVESTIGATION IS NOT COMPLETE AT THIS TIME. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. WE WILL PROVIDE FOLLOW-UP REPORT ONCE MORE INFORMATION IS CONCLUDED FROM THE INVESTIGATION AND CORRECTIVE ACTIONS ARE DETERMINED.

Description of Event or Problem · 0

"IN THE PAST FEW WEEKS, I HAD 2 PATIENTS WITH A RETENTION BLADDER (1X 800CC). ALL 2 OF THESE PATIENTS CAME FROM THE OR AND HAD BEEN IN THE WARD FOR SEVERAL HOURS. BECAUSE THE URINE PRODUCTION PER HOUR WAS LOW, THEY WERE BOTH FILLED SEVERAL TIMES. IN THE LATE SHIFT I FOUND OUT THAT THE BLADDER WAS FULL. WHEN RINSING, THE LIQUID GOES IN EASILY BUT DOES NOT COME OUT. PATIENTS OFTEN INDICATE THAT THEY HAVE THE FEELING THAT THEY HAVE TO AND CLEARLY HAVE A HARDER TIME. WHEN ASKING AROUND, MORE COLLEAGUES NOTICED THIS. I WAS ABLE TO SOLVE IT EVERY TIME BY EMPTYING THE BALLOON AND MOVING IT FURTHER. PREVIOUSLY WE DID 10CC IN THE DECORATION BUT NOWADAYS THERE IS MAX 5CC IN IT, MAYBE THIS IS THE PROBLEM? I HAVE AN AWAKE PATIENT THIS NIGHT WHO HAS THE SENSATION OF A FULL BLADDER AND LESS URINATION (NO RETENTION BLADDER YET). I HAVE NOW ALSO EMPTIED THE BALLOON AND PUSHED THE CATHETER ON, LATER THE PROBLEM HAS BEEN SOLVED, BUT THAT'S WHY I'M GOING TO DIM IT NOW' AFTER ASKING AROUND AT THE OTHER IC'S IN ONE HALF-DAY (WE HAVE 3) WE COME TO TELL THE NEXT ONE; · 3 COLLEAGUE CASE HISTORIES WHERE THE PATIENT HAD ENCOUNTERED RETENTION BLADDER WITH DEROYAL'S URINARY CATHETER. · 4 URINARY CATHETERS THAT LEAK URINE. · 3 TIMES IN A SHORT TIME THAT THE URINARY CATHETER WAS IN BED WITH THE PATIENT FOR NO APPARENT REASON."

Description of Event or Problem · 0

"IN THE PAST FEW WEEKS, I HAD 2 PATIENTS WITH A RETENTION BLADDER (1X 800CC). ALL 2 OF THESE PATIENTS CAME FROM THE OR AND HAD BEEN IN THE WARD FOR SEVERAL HOURS. BECAUSE THE URINE PRODUCTION PER HOUR WAS LOW, THEY WERE BOTH FILLED SEVERAL TIMES. IN THE LATE SHIFT I FOUND OUT THAT THE BLADDER WAS FULL. WHEN RINSING, THE LIQUID GOES IN EASILY BUT DOES NOT COME OUT. PATIENTS OFTEN INDICATE THAT THEY HAVE THE FEELING THAT THEY HAVE TO AND CLEARLY HAVE A HARDER TIME. WHEN ASKING AROUND, MORE COLLEAGUES NOTICED THIS. I WAS ABLE TO SOLVE IT EVERY TIME BY EMPTYING THE BALLOON AND MOVING IT FURTHER. PREVIOUSLY WE DID 10CC IN THE DECORATION BUT NOWADAYS THERE IS MAX 5CC IN IT, MAYBE THIS IS THE PROBLEM? I HAVE AN AWAKE PATIENT THIS NIGHT WHO HAS THE SENSATION OF A FULL BLADDER AND LESS URINATION (NO RETENTION BLADDER YET). I HAVE NOW ALSO EMPTIED THE BALLOON AND PUSHED THE CATHETER ON, LATER THE PROBLEM HAS BEEN SOLVED, BUT THAT'S WHY I'M GOING TO DIM IT NOW' AFTER ASKING AROUND AT THE OTHER IC'S IN ONE HALF-DAY (WE HAVE 3) WE COME TO TELL THE NEXT ONE: 3 COLLEAGUE CASE HISTORIES WHERE THE PATIENT HAD ENCOUNTERED RETENTION BLADDER WITH DEROYAL'S URINARY CATHETER. 4 URINARY CATHETERS THAT LEAK URINE. 3 TIMES IN A SHORT TIME THAT THE URINARY CATHETER WAS IN BED WITH THE PATIENT FOR NO APPARENT REASON."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
560323 FOLEY CATHETER, 400 SERIES 14 FR (+/-0.1C) CATHETER, UPPER URINARY TRACT EYC DEROYAL INDUSTRIES, INC. 81-080414EU 55456566 50749756596652

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown