JuggerKnot Soft Anchors 912029Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00880304522350), received between Nov 27, 2019 and Jul 17, 2025 — classified as 2 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Expulsion” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 17, 2025Expulsion; Expulsion

  IT WAS REPORTED THAT DURING THE SURGERY, THE IMPLANT WAS PULLED OUT UNINTENTIONALLY. THERE WAS NO REPORT OF FOREIGN BODY RETAINED OR HARM TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22529506 ↗
• MalfunctionJan 16, 2024Fracture; Material Fragmentation; Fracture; Material Fragmentation

  NO FURTHER EVENT INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18517811 ↗
• InjuryAug 23, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL PROCEDURE TO REPAIR A SUPRASPINATUS RUPTURE. THERE WAS AN SUBSEQUENT PROCEDURE TO REPAIR THE SUPRASPINATUS AS IT HAD RUPTURED AGAIN. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: Muscle/Tendon Damage

  MAUDE report 15279064 ↗
• MalfunctionJan 31, 2020Migration or Expulsion of Device; Migration or Expulsion of Device

  IT WAS REPORTED THAT DURING SURGERY, THE ANCHOR GOT PULLED OUT FROM BURR HOLE WHEN THE SURGEON PULLED THE SUTURE AFTER IT WAS IMPLANTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9652700 ↗
• InjuryNov 27, 2019Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED THE PATIENT WAS REVISED TO ADDRESS ANCHOR LOOSENING APPROXIMATELY ONE MONTH POST PRIMARY IMPLANTATION. NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORTING.

  Patient problems: Failure of Implant

  MAUDE report 9384321 ↗