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Endo Lube 220-90Recalls & reported problems

Covidien LP · Seal and Instrument Lubrication Kit · Class 2

Data updated Oct 18, 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 20884521066561), received between Aug 14, 2020 and Aug 14, 2020 — 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 18, 2026.

Most reported problems

Device problems

  • Break1
  • Detachment of Device or Device Component1

Patient problems

  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 14, 2020Break; Detachment of Device or Device Component; Break; Detachment of Device or Device Component

    ACCORDING TO THE REPORTER, DURING LAPAROSCOPIC GALLBLADDER OPERATION, WHEN SUPPOSED TO USE THE ULTRASOUND, THE TIP OF THE BOTTLE DIVIDES SO THAT THE UPPER PART FALLS INTO A PORT. THE PORT COULD BE SPLIT AND THE FALLEN PART COULD BE PICKED UP. THERE WAS NO PATIENT INJURY.

    Patient problems: No Information

    MAUDE report 10408583 ↗

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Sources and updates

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