JuggerKnot CM-99129BNRecalls & reported problems
Riverpoint Medical, LLC · Soft Anchor · Class 2 · Implant
All models of JuggerKnot (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00810020087192), received between Feb 18, 2022 and Jan 8, 2024 — classified as 4 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
- Deformation Due to Compressive Stress1
- Device Handling Problem1
- Difficult to Insert1
Patient problems
- Unspecified Infection4
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryJan 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, "A WOUND INFECTION OCCURRED IN 2 DIFFERENT PATIENTS APPROX. 4 WEEKS AFTER THE INSERTION OF JUGGERKNOT ANCHORS. BOTH PATIENTS HAVE THE SAME LOT NUMBER. IT IS NOT CLEAR WHICH OF THE 4 ANCHORS CAUSED THE PROBLEMS."
Patient problems: Unspecified Infection
MAUDE report 18469638 ↗InjuryJan 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, "A WOUND INFECTION OCCURRED IN 2 DIFFERENT PATIENTS APPROX. 4 WEEKS AFTER THE INSERTION OF JUGGERKNOT ANCHORS. BOTH PATIENTS HAVE THE SAME LOT NUMBER. IT IS NOT CLEAR WHICH OF THE 4 ANCHORS CAUSED THE PROBLEMS."
Patient problems: Unspecified Infection
MAUDE report 18469461 ↗InjuryJan 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, "A WOUND INFECTION OCCURRED IN 2 DIFFERENT PATIENTS APPROX. 4 WEEKS AFTER THE INSERTION OF JUGGERKNOT ANCHORS. BOTH PATIENTS HAVE THE SAME LOT NUMBER. IT IS NOT CLEAR WHICH OF THE 4 ANCHORS CAUSED THE PROBLEMS."
Patient problems: Unspecified Infection
MAUDE report 18469216 ↗InjuryJan 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, "A WOUND INFECTION OCCURRED IN 2 DIFFERENT PATIENTS APPROX. 4 WEEKS AFTER THE INSERTION OF JUGGERKNOT ANCHORS. BOTH PATIENTS HAVE THE SAME LOT NUMBER. IT IS NOT CLEAR WHICH OF THE 4 ANCHORS CAUSED THE PROBLEMS."
Patient problems: Unspecified Infection
MAUDE report 18468946 ↗MalfunctionOct 27, 2022Deformation Due to Compressive Stress; Deformation Due to Compressive Stress
ACCORDING TO THE REPORTER, "DURING IMPLANTATION OF THE JUGGERKNOT ANCHOR, THE ENTIRE TIP GOT BROKEN. DELAY 10 MIN."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15680684 ↗MalfunctionSep 28, 2022Difficult to Insert; Difficult to Insert
ACCORDING TO THE REPORTER, "THE ANCHOR WOULD NOT STAY ON INSERTER, THEREFORE WOULD NOT DEPLOY".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15499536 ↗MalfunctionFeb 18, 2022Device Handling Problem; Device Handling Problem
ACCORDING TO THE REPORTER, "2.9 JUGGERKNOTS WERE USED WITH PROPER TECHNIQUE DURING THE PROCEDURE. EACH ITEM ATTACHED FAILED TO PROPERLY DEPLOY WHEN ATTEMPTING TO PLACE ANCHOR INTO THE PATIENT. PRODUCT FAILURE DURING FOOT AND ANKLE SOFT TISSUE REPAIR (MODIFIED BROSTRUM) AND ANKLE SYNDESMOSIS ON (B)(6) 2022".
Patient problems: Insufficient Information
MAUDE report 13564284 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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