JuggerKnot CM-99114BRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00810020087109), received between Oct 27, 2022 and Sep 17, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Break” (3 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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 17, 2026Material Integrity Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50810779 ↗
• MalfunctionJun 17, 2025Material Integrity Problem; Material Integrity Problem

  ACCORDING TO THE REPORTER, "IT WAS REPORTED THAT DURING THE SURGERY, THE TIP OF THE COMPLAINT PRODUCT'S INSERTER WAS FRACTURED DURING USE. AND THE SURGEON FINISHED THE SURGERY WITHOUT REMOVING THE FRACTURED PIECE OF INSERTER, SO THE FRACTURED PIECE OF INSERTER HAS BEEN REMAINED IN THE PATIENT'S BODY."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22243325 ↗
• MalfunctionMar 5, 2024Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem

  ACCORDING TO THE REPORTER, "ANCHOR FAILED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18837008 ↗
• MalfunctionOct 25, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  ACCORDING TO THE REPORTER, "IT WAS REPORTED THAT DURING THE SURGERY, THE ANCHOR OF THIS COMPLAINT PRODUCT COULDN'T BE IMPLANTED LIKE A NORMAL PRODUCT. BY THE WAY, THE SURGEON IS FAMILIAR WITH THIS PRODUCT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18005555 ↗
• MalfunctionMar 1, 2023Break; Break

  ACCORDING TO THE REPORTER, "IT WAS REPORTED THAT DURING THE SURGERY, THE BROADBAND TAPE OF THIS COMPLAINT PRODUCT COULD NOT SLIDE. SUBSEQUENTLY, THE BROADBAND TAPE FRACTURED."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16463827 ↗
• MalfunctionFeb 20, 2023Migration or Expulsion of Device; Migration or Expulsion of Device

  ACCORDING TO THE REPORTER, "IT WAS REPORTED THAT DURING THE SURGERY, TH ANCHOR WAS PULLED OUT ALTHOUGH THE SURGEON IMPLANTED IT FOLLOWING THE NORMAL USAGE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16406086 ↗
• MalfunctionOct 27, 2022Break; Break

  ACCORDING TO THE REPORTER, "THE BROADBAND TAPE OF THIS COMPLAINT PRODUCT WAS BROKEN DURING THE TYING PROCEDURE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15680704 ↗
• MalfunctionOct 27, 2022Break; Break

  ACCORDING TO THE REPORTER, "THE BROADBAND TAPE OF THIS COMPLAINT PRODUCT WAS BROKEN DURING THE TYING PROCEDURE."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15680688 ↗