CleanCoat E3774-36CRecalls & reported problems
Covidien LP · Laparoscopic Wire L-Hook Electrode Coated · 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 10884521550827), received between Jul 11, 2023 and Jul 11, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 11, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
ACCORDING TO THE REPORTER, DURING A LAP APPENDECTOMY, THE NURSE REPORTED THAT SHE HAD NOT OBSERVED THE PLASTIC ELECTRODE PROTECTOR OF THE DEVICE ON THE ELECTRODE SHAFT AS IT WAS POSITIONED BELOW THE BASE OF THE ELECTRODE TIP AND RESEMBLED BEING A PART OF THE SHAFT AND WHEN EXITING THE BODY CAVITY (COMING THROUGH THE TROCAR) UPON PROCEDURE COMPLETION, IT HAD CAME OFF AND WAS SEEN FALLING IN THE PATIENT BODY VIA ENDOSCOPY SCREEN, THE PIECE WAS RETRIEVED WITHOUT AN X-RAY REQUIRED TO ASSIST IN LOCATING THE PIECE AND NO ADDITIONAL MEDICAL/SURGICAL PROCEDURE WAS NEEDED TO REMOVE THE PIECE FROM THE PATIENT. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17302858 ↗
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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 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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