EAGLE SWIFT 286509000Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034212784), received between Jan 10, 2018 and Apr 12, 2021 — classified as 2 malfunctions.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 12, 2021Material Integrity Problem; Material Integrity Problem

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN CANADA AS FOLLOWS: IT WAS REPORTED THAT ON AN UNKNOWN DATE THE STANDARD SCREWDRIVER WAS DAMAGED. IT WAS UNKNOWN HOW IT OCCURRED. THERE WAS NO PROCEDURE AND PATIENT INVOLVEMENTS ARE REPORTED. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR (1) STANDARD SCREWDRIVER. THIS REPORT IS 1 OF 1(B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11653238 ↗
• MalfunctionJan 10, 2018Break; Break

  DR. (B)(6) WAS ASKED FOR THE DRIVER TO FINAL TIGHTEN THE SCREWS (16MM SCREWS, 1 SELF-DRILLING, AND 3 SELF TAPPING) INTO THE SWIFT PLUS PLATE. AS HE TIGHTENED THE TIP BROKE OFF THE DRIVER, DR. (B)(6) WAS ABLE TO GRAB THE BROKEN OFF TIP OUT OF THE PATIENT. HE WAS GIVEN THE THREADED DRIVER TO FINISH TIGHTENING THE SCREWS. BROKEN DRIVER WAS EXAMINED AND IT APPEARS THAT THE TIP JUST SNAPPED OFF.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7178682 ↗