ELEVIEW

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-11-06 for ELEVIEW manufactured by Cosmo Technologies, Ltd..

Event Text Entries

[126305192] Colonoscopy with post procedure para-abdominal pain; a proximal transverse colon perforation was confirmed [procedural intestinal perforation]. Case description: on (b)(6) 2018, a spontaneous report was received from a physician via a company representative regarding a (b)(6) caucasian male who was being treated with eleview (submucosal injection agent). On 25-oct-2018, additional information was received from a physician and the case was assessed as serious and unexpected. Medical history included that the patient was described as "healthy", had colon polyps, a "recent bout" (relative to (b)(6) 2018) of diarrhea and bloody stool which was likely infectious colitis (all had resolved at the time of the procedure); and a ct (computerized tomogram) scan which showed colonic thickening. Concomitant products included: citalopram 20 mg 1x/day, doxazosin 2 mg at bedtime, loratadine 10 mg 1x/day, losartan 50 mg 1x/day, pravastatin 40 mg 1x/day, ranitidine 150 mg 2x/day and dietary supplements of: saw palmetto 160 mg 2x/day and a multivitamin. On (b)(6) 2018, the patient had treatment with eleview at 5 ml for 2 polyps, during a colonoscopy procedure for polypectomies. On (b)(6) 2018, after the eleview was injected under the base of a 1. 5 cm "quite flat" polyp in the proximal transverse colon, the polyp "sort of became a mushroom-shaped lesion. " the polyp lifted off the mucosa, but created a "neck," where the snare tended to settle. This "neck" must have made the "conventional hot" snare be too close to the serosa and caused the snare to cut too deep. After excising the lesion (later identified as sessile serrated adenoma), the patient was sent home. After a few hours, the patient complained of para-abdominal pain and was investigated for a perforation. On (b)(6) 2018, after confirmation of a perforation in the proximal transverse colon, the patient was hospitalized and underwent a hemicolectomy and was treated with unspecified antibiotics. The physician felt that eleview contributed to the perforation. On "approximately" (b)(6) 2018, the patient was discharged and as of 25-oct-2018, was making a full recovery. No additional information was provided. Company comment: keeping in mind the physician's data and opinion provided that eleview contributed by way of the technique of usage, the event of perforation is being reported during the use of eleview. Perforation is a known procedure related risk and an expected occasional adverse event during polypectomy. Also, previous literature has suggested that submucosal agents are protective against perforations by actually providing a cushion type effect. The perforation is most likely due to a user error with the other equipment used (for example the snare) rather than the eleview itself. Event assessment: perforation - serious. Reportable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3013045306-2018-00001
MDR Report Key8043181
Date Received2018-11-06
Date of Report2018-10-07
Date of Event2018-08-31
Date Facility Aware2018-10-07
Report Date2018-10-11
Date Reported to Mfgr2018-10-11
Date Added to Maude2018-11-06
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELEVIEW
Generic NameSUBMUCOSAL INJECTION AGENT
Product CodePLL
Date Received2018-11-06
Lot NumberUH143
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age14 MO
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOSMO TECHNOLOGIES, LTD.
Manufacturer AddressRIVERSIDE II SIR JOHN ROGERSON'S QUAY DUBLIN 2, D02KV60 EI D02KV60


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other 2018-11-06

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