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UNIVERSAL PLUS 60-5272-127Recalls & reported problems

Conmed Corporation · UNIVERSAL PLUS LAPAROSCOPIC ELECTRODE WITH SUCTION/IRRIGATION, L-HOOK 5 MM X 27 CM · Class 2

All models of UNIVERSAL PLUS (9)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30653405010603), received between Feb 26, 2020 and Feb 26, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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

  • Material Fragmentation1

Patient problems

  • Injury1

Recent adverse event reports

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

  • InjuryFeb 26, 2020Material Fragmentation; Material Fragmentation

    THE CUSTOMER REPORTED THAT THE DEVICE, 60-5272-127, WAS BEING USED DURING AN UNKNOWN TYPE OF SURGERY ON (B)(6) 2020 WHEN THE "TIP BROKE OFF IN PATIENT. NOT SURE EXTENT OF INJURY UNTIL THEY CAN EVALUATE". A GOOD FAITH EFFORT HAS BEEN COMPLETED TO OBTAIN MORE INFORMATION; HOWEVER, NO RESPONSE HAS BEEN RECEIVED FROM THE CONTACT OF THE FACILITY TO DATE. THIS REPORT IS BEING RAISED ON THE BASIS OF INJURY DUE TO ALLEGATIONS OF INJURY BY THE REPORTER WITH NO FURTHER CONTACT OR INFORMATION.

    Patient problems: Injury

    MAUDE report 9757283 ↗

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Sources and updates

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