inforMED
MalfunctionEXS

SENSICA UO MONITOR ICU

Received Mar 1, 2023 · Event occurred Feb 8, 2023

Report 1018233-2023-01314 · MDR key 16459473

Device

Generic name

Sensica Device

Model number

SCCS1002

Catalog 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

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. THE UNIT WAS MISSING A SCREW ON THE BOTTOM PLATE. PER REVIEW OF WO ON 20FEB2023, THERE WAS NO PATIENT INVOLVEMENT.

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 UNIT WAS MISSING A SCREW ON THE BOTTOM PLATE. PER REVIEW OF WO ON 16FEB2023, THERE WAS NO PATIENT INVOLVEMENT.

Additional Manufacturer Narrative

UPON FURTHER REVIEW, BD HAS DETERMINED THAT THIS MDR WAS REPORTED IN ERROR AS THE FAILURES OCCURRED TO UNITS WHILE IN BD CONTROL THAT HAD NOT BEEN RELEASED FROM THE GDC/INVENTORY WOULD NOT REQUIRE COMPLAINTS. 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.