STIEGMANN-GOFF 000221Recalls & reported problems
Conmed Corporation · STIEGMANN-GOFF CLEARVUE Endoscopic Ligator, 5 Disposable Cylinders · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10653405053651), received between May 23, 2019 and May 23, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 23, 2019Break; Break
THE CONMED REPRESENTATIVE REPORTED ON BEHALF OF THE FACILITY THAT THE 000221, CLEAR LIGATOR 5 BAND KIT, BROKE DURING AN EGD ON (B)(6) 2019. HE REPORTED THAT THE DOCTOR WAS DOING ESOPHAGEAL BANDING AND THE BAND BROKE OFF AND HE HAD TO FISH OUT WITH A NET. THE PROCEDURE WAS COMPLETED USING ANOTHER OF THE SAME PRODUCT. THERE WAS NO REPORTED DELAY IN PROCEDURE. THERE WAS NO PATIENT INJURY REPORTED, ALTHOUGH THE BAND ALMOST WENT INTO THE PATIENT'S LUNG. THIS REPORT IS BEING RAISED AS DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8636061 ↗
Other Ligator, esophageal devices
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- Saeed G22692Cook Incorporated · Ligator, esophageal295 reports
- SINGLE USE LIGATING DEVICE HX-400U-30Olympus Medical Systems Corp. · Ligator, Esophageal1 recall239 reports
- Saeed G22553Cook Incorporated · Ligator, esophageal289 reports
- Saeed G31917Cook Incorporated · Ligator, esophageal123 reports
- SINGLE USE LIGATING DEVICE HX-400U-30Olympus Medical Systems Corp. · Ligator, Esophageal97 reports
- Single Use Rotatable Clip Fixing Device HX-201UR-135Olympus Medical Systems Corp. · Ligator, esophageal1 recall1 death10 reports
- Single Use Rotatable Clip Fixing Device HX-201UR-135LOlympus Medical Systems Corp. · Ligator, esophageal1 recall8 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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