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Valleylab SEL7010Recalls & reported problems

Covidien LP · Laparoscopic Smoke Evacuation System Active and Passive · Class 1

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 10884521740860), received between Dec 12, 2022 and Dec 12, 2022 — 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. How this data works · Data updated Oct 13, 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.

  • MalfunctionDec 12, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    ACCORDING TO THE REPORTER, DURING A PROCEDURE, THE TUBE PART OF THE CONNECTOR ON THE TROCAR VALVE SIDE CAME OFF. SO, IT WAS REPLACED WITH A DIFFERENT ONE OF THE SAME PRODUCT. IT WAS REPORTED THAT THE BROKEN PIECE DID NOT FALL INTO THE PATIENT'S CAVITY. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15960114 ↗

Other Tubing/tubing with filter, insufflation, laparoscopic devices

All Tubing/tubing with filter, insufflation, laparoscopic devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.