inforMED
MalfunctionFCK

RBI2 SUCTION RECTAL BIOPSY SYSTEM

Received Dec 14, 2024 · Event occurred Sep 27, 2024

Report 3005921952-2024-00005 · MDR key 20934278

Device

Generic name

Rbi2

Model number

RBI2

Catalog number

CP1200

Lot number

U22318

Product problems

  • Misassembly by Users
  • No Apparent Adverse Event
  • Misassembly by Users
  • No Apparent Adverse Event

Patient

1 MO · Female

  • No Clinical Signs, Symptoms or Conditions
  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

EXAMINATION OF CAPSULE: BLADE, HOLE SHAPE, AND HOLDING SLOTS WERE INSPECTED. DIMENSIONS MATCHED SPECIFICATIONS PER DRAWING # 0005-AUS REV.1, WITHIN TOLERANCE LEVELS. VISUAL INSPECTION SHOWED NO SIGNS OF THE CAPSULE BEING TWISTED TO LOCK ON POSITION. FUNCTION TESTING: CAPSULE FROM LOT # 22318 WAS PLACED ONTO A HP1000 AND TWISTED AND IT SECURELY LOCKED ONTO THE LUGS. THE CAPSULE FIRED NORMALLY, ENGAGING WITH THE CUTTING BOARD, WITH CUTTING BOARD CUT RESISTANCE WITHIN NORMAL PARAMETERS. ACTIVATION ISSUE: THE CAPSULE HAD NOT BEEN ACTIVATED DURING USE, AND THE INNER PISTON WAS UNABLE TO PUSH OR FIRE THE BLADE DUE TO THE CAPSULE NOT BEING LOCKED ONTO HP1000 LOCKING LUGS. THE CLICKING NOISE MENTIONED BY THE OPERATOR SUGGESTS THE TRIGGER WAS ACTIVATED AND COMPLETELY PUSHED THE CAPSULE OFF THE HP1000. ROOT CAUSE ANALYSIS: BLADE FUNCTIONALITY: THE BLADE WAS NOT FIRED, DID NOT LEAVE ITS ASSEMBLED POSITION, AND COULD NOT PHYSICALLY ENGAGE WITH THE MUCOSA WALL. DESIGN CONSIDERATIONS: ONCE FIRED, THE BLADE DESIGN ENSURES IT CANNOT RETRACT AND REMAINS IN THE FIRED POSITION. THIS EXPLAINS WHY THE CAPSULE COULD BE REMOVED SUCCESSFULLY AFTER THE PATIENT PASSED STOOL. OPERATIONAL OVERSIGHT: THE CAPSULE WAS NOT TWISTED AND LOCKED PROPERLY ONTO THE HANDPIECE DURING INITIAL USE. INSTEAD, IT WAS LIKELY PUSHED FORWARD INTO THE PATIENT DUE TO IMPROPER MOUNTING. UPON PATIENT STOOLING, THE CAPSULE WAS PUSHED OUT BECAUSE THE BLADE REMAINED INACTIVE, RESULTING IN NO TISSUE CAPTURE OR BLEEDING. CONCLUSION: THE FAILURE WAS CAUSED BY THE CAPSULE NOT BEING TWISTED AND LOCKED ONTO THE HANDPIECE, LEADING TO IMPROPER DEPLOYMENT DURING USE. THIS MECHANICAL OVERSIGHT PREVENTED THE BLADE FROM FIRING, CONFIRMING NO FAULT IN THE CAPSULE'S DESIGN OR MANUFACTURING. PROPER LOCKING AND ACTIVATION PROCEDURES SHOULD RESOLVE SUCH ISSUES IN FUTURE USE.

Description of Event or Problem

SUCTION RECTAL BIOPSY WAS PERFORMED SUCCESSFULLY X2. ON THE THIRD ATTEMPT AFTER TRIGGERING THE SUCTION RECTAL BIOPSY GUN THERE WAS A CLICKING NOISE. THE CAPSULE WAS UNABLE TO BE REMOVED FROM PT'S RECTUM AND FOUND TO BE STUCK ON RECTAL MUCOSA. DR, PED SURG FELLOW NOTIFIED. SHE ATTEMPTING TO FLUSH AND PROBE THE CAPSULE. AFTER ABOUT 40 MINUTES IT WAS SUCCESSFULLY REMOVED AFTER PATIENT STOOLED ON THEIR OWN. NO TISSUE NOTED IN CARTRIDGE ON REMOVAL. NO BLEEDING.