NA 710201Recalls & reported problems
US Endoscopy · Quick Catch in-line suction polyp trap is used for suction retrieval of endoscopically removed polyps. · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00724995184704), received between Jun 20, 2022 and Dec 12, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Component Missing” (2 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
- Component Missing2
- Insufficient Device Problem Information1
- Suction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 12, 2025Component Missing; Component Missing
THE USER FACILITY REPORTED VIA MEDWATCH MW5177901 THAT THE INLINE SUCTION COMPONENT WAS MISSING FROM THEIR QUICK CATCH IN-LINE SUCTION POLYP TRAP. AS A RESULT, THE POLYP COULD NOT BE RETRIEVED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23793278 ↗MalfunctionAug 28, 2025Suction Problem; Suction Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE POLYP WAS NOT PROPERLY SUCTIONED THROUGH THEIR QUICK CATCH IN-LINE SUCTION POLYP TRAP RESULTING IN A PROCEDURE DELAY. THE POLYP WAS UNABLE TO BE LOCATED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22913404 ↗MalfunctionDec 1, 2023Component Missing; Component Missing
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, A NURSE OBSERVED THAT THE SCREEN WAS MISSING FROM THE QUICK CATCH IN-LINE SUCTION POLYP TRAP SUBSEQUENTLY CAUSING THE REMOVED POLYP TO BECOME LODGED IN THE MANIFOLD OF THE SUCTION DEVICE. THE PATIENT PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A PROCEDURE DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18247342 ↗MalfunctionJun 20, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
THE USER FACILITY REPORTED VIA USER FACILITY MEDSUN REPORT THE FOLLOWING, "TRAP USED TO CATCH SNARED POLYPS DID NOT HAVE NETTING AND DID NOT CATCH RESECTED POLYP. POLYP HAD TO BE FISHED OUT OF SUCTION CANISTER AND COULD HAVE BEEN LOST WITHOUT ABILITY OF PATHOLOGY TO EXAMINE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14748938 ↗
Other BOTTLE, COLLECTION, VACUUM devices
- OASIS 3600-100Atrium Medical Corporation · Bottle, Collection, Vacuum3 recalls1 death175 reports
- OCEAN 2002-000Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM3 recalls44 reports
- EXPRESS 16400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall110 reports
- EXPRESS 4000-100NAtrium Medical Corporation · Bottle, Collection, Vacuum2 recalls30 reports
- OCEAN 2002-400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM2 recalls18 reports
- OASIS 3612-100Atrium Medical Corporation · Bottle, Collection, Vacuum1 recall18 reports
- Medline DYNDSCL1500Medline Industries, Inc. · BOTTLE, COLLECTION, VACUUM1 recall13 reports
- PNEUMOSTAT 16100Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall3 deaths12 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.