OLYMPUS
Received Mar 17, 1998 · Event occurred Feb 9, 1998
Report 9610773-1998-00004 · MDR key 156628
Device
Generic name
Obturator
Manufacturer
Olympus Winter & Ibe GmbhModel number
A2637Catalog number
83A2637
Lot number
76W
Patient
UNKNOWN
Narrative
Description of Event or Problem
DURING A BLADDER TUMOR RESECTION PROCEDURE, THE FLEXIBLE TIP OF THE A2637 OBTURATOR FROZE IN AN UPWARD DEFLECTIVE POSITION AFTER BEING INSERTED INTO THE PT. WHEN THE SURGEON WAS UNSUCCESSFUL IN HIS ATTEMPTS TO REMOVE THE OBTURATOR FROM THE INFLOW SHEATH, HE EXERTED ADD'L PRESSURE WHICH CAUSED THE CERAMIC BEAK OFF THE INFLOW SHEATH AT THE TIP WHILE THE DEVICE WAS INSIDE THE PT. ALTHOUGH THE SURGEON ATTEMPTED TO RETRIEVE THE CERAMIC TIP, THE PIECE WAS NOT IN VIEW AFTER THE INSTRUMENTATION HAD BEEN REMOVED. THE SURGEON IS UNSURE WHETHER THE PIECE OR MULTIPLE PIECES WILL PASS WITHOUT ASSISTANCE BUT ADD'L SURGICAL INTERVENTION WAS NOT PERFORMED. A SECOND COMPLICATION DEVELOPED AS THE SURGEON ATTEMPTED TO WITHDRAW THE INSTRUMENTATION. AS HE PLACED HIS HANDS ON THE OBTURATOR AND THE PT, AND DUE TO THE AMOUNT OF FORCE BEING EXERTED, THE SURGEON INADVERTENTLY PUSHED THE ENTIRE INSTRUMENT ASSEMBLY FORWARD APPARENTLY CAUSING PERFORATION OF THE URETHRAL WALL. EVENTUALLY, THE SURGEON REMOVED THE INSTRUMENT ASSEMBLY AND COMPLETED THE ORIGINAL PROCEDURE WITH A SECOND SET OF EQUIPMENT. THE PERFORATION WAS NOT REPAIRED SINCE THIS TYPE OF PERFORATION NORMALLY HEALS WITHOUT INTERVENTION. HOWEVER, THE PT EXPERIENCED BLEEDING AS A RESULT OF THE PROCEDURE AND OVERNIGHT HOSPITALIZATION WAS REQUIRED. PRIOR TO THE PROCEDURE, THE PT WAS PLACED ON ANTIBIOTICS. ANTIBIOTICS WERE CONTINUED FOLLOWING THIS EVENT. AS OF 2/26/98, THE PT'S CONDITION WAS REPORTEDLY GOOD. THE PT IS SCHEDULED FOR A TRANS URETHRAL RESECTION PROCEDURE DUE TO REASONS POTENTIALLY UNRELATED TO THIS EVENT.
Additional Manufacturer Narrative
UPON EVAL, THE MFR FOUND THAT THE EPOXY CEMENT USED TO SECURE AN INTERNAL SCREW IN THE DEFLECTING TIP OF THE OBTURATOR HAD DETERIORATED OVER TIME. THIS ALLOWED THE SCREW TO SHIFT, AND AS A RESULT, THE OBTURATOR LOCKED IN A DEFLECTED POSITION. TO COUNTER THIS PHENOMENON, THE MFR HAS VALIDATED A CHANGE TO A LASER WELDING PROCESS.