SENSICA URINE OUTPUT SYSTEM
Received Feb 22, 2023 · Event occurred Feb 1, 2023
Report 1018233-2023-01095 · MDR key 16417800
Device
Generic name
Sensica Urine Output System
Manufacturer
C.r. Bard, Inc. (covington) -1018233Model number
SCCS1002Catalog number
SCCS1002
Lot number
NA
Product problems
- Device Sensing Problem
- Device Sensing Problem
Patient
Unknown
- No Clinical Signs, Symptoms or Conditions
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED THAT THE TUBE SENSOR LEFT ENTRY READS ¿OPEN¿ WHEN BAG TUBE WAS NOT ATTACHED. ENSURED THE TUBE SENSOR LEFT¿ ENTRY READS ¿ACTUATED¿ AFTER BAG TUBE WAS CONNECTED ON THE SENSICA URINE OUTPUT SYSTEM. DURING THE EXECUTE FILED ACTION PER REQUIREMENTS REPROCESSING PROTOCOL SENSICA TOUCHSCREEN FIRMWARE UPDATE FIELD ACTION, TO ADDRESS DEVICE PERFORMANCE ISSUES RELATED TO PHANTOM TOUCHES THAT MIGHT OCCUR AFTER CLEANING WITH CLEANING OR DISINFECTING WIPES AND TO INACCURATE VOLUME MEASUREMENTS. THE TUBE SENSOR LEFT FAILED AND SHOWED ACTUATED WITH NO TUBE INSTALLED. PER REVIEW OF WO ON 16FEB2023, THERE WAS NO PATIENT INVOLVEMENT.
Additional Manufacturer Narrative
THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE A SUPPLEMENTAL REPORT WILL BE FILED.
Description of Event or Problem
IT WAS REPORTED THAT THE TUBE SENSOR LEFT ENTRY READS ¿OPEN¿ WHEN BAG TUBE WAS NOT ATTACHED. ENSURED THE TUBE SENSOR LEFT¿ ENTRY READS ¿ACTUATED¿ AFTER BAG TUBE WAS CONNECTED ON THE SENSICA URINE OUTPUT SYSTEM. DURING THE EXECUTE FILED ACTION PER REQUIREMENTS REPROCESSING PROTOCOL SENSICA TOUCHSCREEN FIRMWARE UPDATE FIELD ACTION, TO ADDRESS DEVICE PERFORMANCE ISSUES RELATED TO PHANTOM TOUCHES THAT MIGHT OCCUR AFTER CLEANING WITH CLEANING OR DISINFECTING WIPES AND TO INACCURATE VOLUME MEASUREMENTS. THE TUBE SENSOR LEFT FAILED AND SHOWED ACTUATED WITH NO TUBE INSTALLED. PER REVIEW OF WO ON 16FEB2023, THERE WAS NO PATIENT INVOLVEMENT.
Additional Manufacturer Narrative
UPON FURTHER REVIEW, BD HAS DETERMINED THAT THIS MDR WAS INITIALLY REPORTED IN ERROR AS THIS EVENT IS NOT REPORTABLE. H11: SECTION A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT/REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO BD.