Valleylab E3305 (UDI 20884521039077)Recalls & reported problems
Covidien LP · Suction Coagulator · Class 2
Data updated Oct 13, 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 20884521039077), received between Aug 14, 2019 and Aug 14, 2019 — classified as 1 malfunction.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 14, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, DURING ADENOIDECTOMY, AN AREA OF INSULATION ON THE SUCTION BOVIE ELECTRODE WAS SEEN TO HAVE FAILED. THE SURGEON EXAMINED THE PATIENT¿S SURGICAL SIGHT AND NOTICED AN AREA OF APPROXIMATELY 4.6 MM ADJACENT TO THE SURGICAL SIDE THAT HAD UNINTENTIONAL ABLATION/CAUTERIZATION CAUSED BY THE FAILED INSULATION. PATIENT¿S PROCEDURE COMPLETED WITH NEW SUCTION CAUTERY WAND.
Patient problems: Burn(s)
MAUDE report 8893942 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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