JuggerKnot® 912036RRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887868561344), received between Jun 25, 2025 and Jun 25, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fracture” (2 reports).

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.

• MalfunctionJun 25, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING AN INITIAL PROCEDURE TO REPAIR AN UNSTABLE JOINT, THE JUGGER KNOT SHANK BIT WAS USED WITH THE REUSABLE CURVED GUIDE. SUBSEQUENTLY, THE TIP OF THE SHANK BIT HAD FRACTURED. A SECOND SHANK BIT WAS USED AND ALSO FRACTURED. NO PATIENT CONSEQUENCES WERE REPORTED AS A RESULT OF THE EVENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22330818 ↗
• MalfunctionJun 25, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING AN INITIAL PROCEDURE TO REPAIR AN UNSTABLE JOINT, THE JUGGER KNOT SHANK BIT WAS USED WITH THE REUSABLE CURVED GUIDE. SUBSEQUENTLY, THE TIP OF THE SHANK BIT HAD FRACTURED. A SECOND SHANK BIT WAS USED AND ALSO FRACTURED. NO PATIENT CONSEQUENCES WERE REPORTED AS A RESULT OF THE EVENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22330815 ↗