JuggerKnot Soft Anchors 912030Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
All models of JuggerKnot Soft Anchors (15)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 00880304477193), received between Jun 29, 2020 and Sep 29, 2026 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Fracture” (10 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture10
- Expulsion2
- Device Contaminated During Manufacture or Shipping1
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Failure of Implant3
- Insufficient Information2
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Fracture
Patient problems: Insufficient Information
MAUDE report 50938417 ↗MalfunctionSep 29, 2026Fracture
Patient problems: Insufficient Information
MAUDE report 50938397 ↗MalfunctionJan 12, 2026Device Contaminated During Manufacture or Shipping
IT WAS REPORTED THAT THE DISTRIBUTORSHIP FOUND THE PRODUCT TO BE NONCONFORMING AS THE PACKAGE WAS CONTAMINATED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24044553 ↗MalfunctionDec 29, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT AN UNKNOWN ISSUE OCCURRED WITH THE DEVICE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23907285 ↗MalfunctionJul 2, 2025Fracture; Fracture
IT WAS REPORTED THAT DURING THE SURGERY, THE TIP OF THE INSERTER FRACTURED DURING USE. THE SURGERY WAS COMPLETED SUCCESSFULLY AND THE FRACTURED PIECE OF THE INSERTER WAS REMOVED FROM THE PATIENT. THE CASE WAS COMPLETED WITHOUT ANY ADVERSE OUTCOMES TO THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22390953 ↗MalfunctionJul 12, 2024Fracture; Fracture
IT WAS REPORTED THAT DURING A TENDON REPAIR PROCEDURE, THE METAL TIP OF THE ANCHOR BROKE OFF DURING INSERTION. THE FRACTURED PIECES WERE REMOVED FROM THE PATIENT. THERE WAS A SURGICAL DELAY OF TEN MINUTES TO RETRIEVE ADDITIONAL ANCHORS TO COMPLETE THE PROCEDURE HOWEVER THERE WAS NO PATIENT IMPACT AS A RESULT OF THE MALFUNCTION. IT WAS REPORTED THAT NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19729997 ↗MalfunctionSep 7, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 17699806 ↗MalfunctionFeb 23, 2023Fracture; Expulsion; Fracture; Expulsion
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 16428679 ↗MalfunctionFeb 23, 2023Fracture; Expulsion; Fracture; Expulsion
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Failure of Implant
MAUDE report 16428287 ↗MalfunctionJul 12, 2022Fracture; Fracture
IT WAS REPORTED THAT DURING SURGERY, THE TIP OF THE INSERTER FRACTURED. NO PIECES WERE RETAINED BY THE PATIENT AND NO REPORTED CONSEQUENCES OCCURRED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14989382 ↗MalfunctionNov 12, 2020Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10830420 ↗MalfunctionJun 29, 2020Fracture; Fracture
IT WAS REPORTED THE ANCHOR SUTURE BROKE. NO IMPACT TO PATIENT, NO SURGICAL DELAY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10205236 ↗
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- GII QUICKANCHOR ETHIBOND 212034Medos International Sàrl · STAPLE, FIXATION, BONE98 reports
- GII QUICKANCHOR ORTHOCORD 222983Medos International Sàrl · STAPLE, FIXATION, BONE94 reports
- Speed SE-0910Synthes GmbH · Staple, Fixation, Bone1 recall24 reports
- Speed Shift SE-2020-10Synthes GmbH · Staple, Fixation, Bone1 recall10 reports
- Lapiplasty SpeedPlate SK50Treace Medical Concepts, Inc. · Staple, Fixation, Bone59 reports
- Speed SE-1512Synthes GmbH · Staple, Fixation, Bone1 recall6 reports
- LUPINE ORTHOCORD 210709Depuy Mitek, LLC · STAPLE, FIXATION, BONE56 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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