eTrap 00711099Recalls & reported problems
US Endoscopy · The single use eTrap – polyp trap is used for suction retrieval of endoscopically removed polyps. · Class 2
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00724995184728), received between Mar 20, 2024 and Sep 26, 2024 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Suction Problem” (7 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Suction Problem7
- Adverse Event Without Identified Device or Use Problem1
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2024No Apparent Adverse Event; No Apparent Adverse Event
THE USER FACILITY REPORTED VIA VIGILANCE REPORT THAT AN INSECT WAS FOUND INSIDE OF ETRAP POLYP TRAP PACKAGING WHEN OPENED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20317032 ↗MalfunctionSep 19, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT POLYPS WERE LOST IN THEIR ETRAP-POLYP TRAP SUBSEQUENTLY RESULTING IN A PROCEDURE DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20263224 ↗MalfunctionSep 18, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEY WERE LOSING POLYPS RESULTING IN A PROCEDURE DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20250720 ↗MalfunctionAug 29, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEY WERE LOSING POLYPS AS THE POLYPS WERE GOING OVER THE LID WHILE UTILIZING AN ETRAP POLYP TRAP. USER FACILITY PERSONNEL CHANGED SCOPING METHODS TO COMPLETE THE PROCEDURE RESULTING IN A DELAY. THE PROCEDURE WAS COMPLETED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20101440 ↗MalfunctionAug 29, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE SUCTIONED POLYPS COULD NOT BE LOCATED IN THE CANNISTER. USER FACILITY PERSONNEL HAD TO SIFT THROUGH THE CANNISTER TO LOCATE THE POLYPS RESULTING IN A PROCEDURE DELAY. THE PATIENT PROCEDURE WAS COMPLETED SUCCESSFULLY, AND NO INJURIES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20099903 ↗MalfunctionAug 22, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE POLYPS WERE COMING OUT OF THE SUCTION CONTAINER. THE USER FACILITY STATED THAT AT LEAST TWELVE POLYPS WERE LOST. IT IS UNKNOWN IF THE USER FACILITY WAS ABLE TO RETRIEVE ANY OF THE POLYPS. THERE WAS A REPORT OF A PROCEDURE DELAY AS A RESULT OF THE EVENT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20044160 ↗MalfunctionAug 22, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, ONE OF THEIR POLYPS "JUMPED OVER THE INSIDE OF THE TRAP." THE USER FACILITY STATED THAT THE POLYP WAS LOST IN THE SUCTION LINER. THERE WAS A REPORT OF A PROCEDURE DELAY AS A RESULT OF THE EVENT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20040049 ↗MalfunctionJul 17, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THAT POLYPS WERE COMING OUT OF THE SCREEN OF THEIR ETRAP POLYP TRAP. CUSTOMER STATED THAT THE DRAWER OF THE ETRAP POLYP TRAP WAS INSERTED PROPERLY. THERE WAS A REPORT OF A PROCEDURE DELAY AS A RESULT OF THE EVENT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19767728 ↗MalfunctionMar 20, 2024Suction Problem; Suction Problem
THE USER FACILITY REPORTED DURING A PATIENT PROCEDURE THAT THE SUCTION CUPS ON THEIR ETRAP POLYP TRAP DID NOT SEAL PROPERLY. IT HAS BEEN REPORTED THE FACILITY WAS ABLE TO RETRIEVE THE POLYP AND DISCARDED AFTER USE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18946841 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.