Skip to content

Frigitronincs 126Recalls & reported problems

Coopersurgical, Inc. · Cataract, Straight Probe. Tip: 1.0mm length x 1.8mm diameter. Shaft: 27mm length x 1.8mm diameter. · Class 2

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 00888937004212), received between Mar 25, 2021 and Mar 25, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Structural Problem” (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

  • Structural Problem1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionMar 25, 2021Structural Problem

    CUSTOMER STATED: "LEAK". 1216677-2021-00051-1 126 N20 CATARACT PRB STRT (B)(4)

    Patient problems: Insufficient Information

    MAUDE report 11569989 ↗

Other Unit, Cryotherapy, Ophthalmic devices

All Unit, Cryotherapy, Ophthalmic devices →

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