Skip to content

GAMMA 3520-1420SRecalls & reported problems

Stryker GmbH · Long Nail Kit R1.5, Ti, LEFT · Class 2 · Implant

All models of GAMMA (249)

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 07613252274162), received between Sep 8, 2022 and Sep 8, 2022 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Break1
  • Fracture1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjurySep 8, 2022Break; Fracture; Break; Fracture

    IT WAS REPORTED BY PATIENT'S ATTORNEY AS A RESULT OF A LEGAL CLAIM THAT ALLEGEDLY ON (B)(6) 2020 THE PATIENT UNDERWENT SURGERY TO REPAIR A RIGHT SUBTROCHANTERIC FEMUR FRACTURE HE SUSTAINED IN AN AUTOMOBILE ACCIDENT. IT IS FURTHER ALLEGED THAT THE GAMMA NAIL BROKE AT THE LAG SCREW AND WAS REVISED ON (B)(6) 2021.

    Patient problems: Failure of Implant

    MAUDE report 15377746 ↗

Other ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices

All ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page