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Oph.Spatula 08-14527Recalls & reported problems

Katena Products, Inc. · Shepherd Tomahawk Chopper, RH Dominant · Class 1

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 00852979003397), received between Oct 10, 2019 and Oct 10, 2019 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1
  • Fracture1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryOct 10, 2019Break; Fracture; Break; Fracture

    DURING PHACOEMULSIFICATION CATARACT SURGERY THE TIP OF AN OPHTHALMIC CHOPPER BROKE OFF IN THE PATIENT'S EYE. THE SURGEON REMOVED THE BROKEN TIP DURING THE SURGERY.

    Patient problems: Foreign Body In Patient

    MAUDE report 9176998 ↗

Other Spatula, ophthalmic devices

All Spatula, ophthalmic devices →

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