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Synergetics 30.08.25Recalls & reported problems

Synergetics USA, Inc. · 25ga Soft Tip Cannula · Class 1

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 10841305101422), received between Feb 9, 2017 and Feb 9, 2017 — 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 16, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionFeb 9, 2017Break; Break

    WHILE INSERTING THE SILICONE TIP INTO THE ALCON VALVED TROCAR THE TIP SEVERED OFF AND WENT INTO THE PATIENT'S EYE. THE TIP WAS REMOVED AND A BACKUP CANNULA WAS USED WITH NO OTHER ISSUE. THE SURGERY WAS COMPLETED WITH NO INJURY TO THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6314596 ↗

Other INSTRUMENT, MANUAL, SURGICAL, GENERAL USE devices

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Sources and updates

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