JUGGERKNOT 912073Recalls & reported problems
Biomet Orthopedics, LLC · Class 2
Data updated Oct 16, 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 00880304858992), received between Nov 18, 2019 and Jan 12, 2023 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Packaging Problem” (11 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
Device problems
- Packaging Problem11
- Unsealed Device Packaging10
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions11
- No Information1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 12, 2023Packaging Problem; Packaging Problem
IT WAS REPORTED THAT WHEN THE STERILE PACKAGING WAS GOING TO BE OPENED THERE WAS A FOREIGN SUBSTANCE FOUND INSIDE THE STERILE PACKAGING OF THE PRODUCT. THE SURGEON DID NOT USE THE PRODUCT. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16147582 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825449 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825446 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825443 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825423 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825422 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825418 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825416 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825411 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825408 ↗MalfunctionMay 14, 2021Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11825060 ↗MalfunctionNov 18, 2019Material Deformation; Material Deformation
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Information
MAUDE report 9336216 ↗
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- FOOTPRINT 72202901Smith & Nephew, Inc. · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE721 reports
- RIGIDLOOP 232447Medos International Sàrl · FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE633 reports
- 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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