JuggerKnot CM-99429BRecalls & reported problems
Riverpoint Medical, LLC · Soft Anchor · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810020087314), received between Aug 4, 2022 and Mar 19, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Activation, Positioning or Separation Problem1
- Difficult to Open or Remove Packaging Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 19, 2024Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem
ACCORDING TO THE REPORTER, "FAILURE OF SUTURE LOCKING MECHANISM IN ANCHOR."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18935079 ↗MalfunctionAug 4, 2022Difficult to Open or Remove Packaging Material; Difficult to Open or Remove Packaging Material
ACCORDING TO THE REPORTER, "CIRCULATING NURSE OPENED THE JUGGERKNOT USING THE STANDARD STERILE TECHNIQUE. THE SUTURES FELL OUT BEYOND THE STERILE PACKAGING AND THE TECH WAS NOT ABLE TO TRANSFER TO THE BACK TABLE AS THE ANCHOR WAS NOW UNSTERILE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15170655 ↗
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- FOOTPRINT 72202901Smith & Nephew, Inc. · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE721 reports
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- Arthrex® AR-3636Arthrex, Inc. · Fastener, fixation, nondegradable, soft tissue624 reports
- OMNISPAN ORTHOCORD 228141Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE609 reports
- TRUESPAN ORTHOCORD 228162Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE460 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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