Taperloc Complete Micro Primary Femoral 51-108070Recalls & reported problems
Biomet Orthopedics, LLC · Class 2 · Implant
All models of Taperloc Complete Micro Primary Femoral (35)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00880304515291), received between Jul 28, 2022 and Mar 10, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (4 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
- Manufacturing, Packaging or Shipping Problem4
- Packaging Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 10, 2025Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT THE STERILE PACKAGING WAS FOUND DAMAGED. THERE IS NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21558533 ↗MalfunctionNov 6, 2023Packaging Problem; Packaging Problem
NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18078904 ↗MalfunctionApr 21, 2023Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED BY THE DISTRIBUTORSHIP THAT THE PRODUCTS WERE FOUND TO BE NONCONFORMING. THE INCOMING INSPECTION TEAM MEMBER FOUND DEBRIS IN THE STERILE PACKAGE. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16786060 ↗MalfunctionFeb 21, 2023Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT UPON INCOMING INSPECTION, DEBRIS WAS FOUND IN THE STERILE PACKAGING. THERE WAS NO PATIENT INVOLVEMENT. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16408797 ↗MalfunctionNov 18, 2022Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED BY THE DISTRIBUTOR THAT THE PRODUCT WAS FOUND TO BE NONCONFORMING. THEIR INSPECTION TEAM FOUND DEBRIS IN THE STERILE PACKAGE. THERE WAS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15826077 ↗MalfunctionJul 28, 2022Packaging Problem; Packaging Problem
IT WAS REPORTED THAT DURING INCOMING INSPECTION, THE STERILE PACKAGING WAS FOUND TO BE DAMAGED. IT IS UNKNOWN IF THE STERILITY OF THE DEVICE HAS BEEN COMPROMISED. THERE WAS NO PATIENT INVOLVEMENT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15120561 ↗
Other PROSTHESIS, TOE, CONSTRAINED, POLYMER devices
- Taperloc Complete Micro Primary Femoral 51-109070Biomet Orthopedics, LLC · PROSTHESIS, TOE, CONSTRAINED, POLYMER24 reports
- Taperloc Complete Micro Primary Femoral 51-106100Biomet Orthopedics, LLC · PROSTHESIS, TOE, CONSTRAINED, POLYMER13 reports
- Taperloc Complete Micro Primary Femoral 51-109080Biomet Orthopedics, LLC · PROSTHESIS, TOE, CONSTRAINED, POLYMER9 reports
- Taperloc Complete Micro Primary Femoral 51-106180Biomet Orthopedics, LLC · PROSTHESIS, TOE, CONSTRAINED, POLYMER7 reports
- Taperloc Complete Micro Primary Femoral 51-106120Biomet Orthopedics, LLC · PROSTHESIS, TOE, CONSTRAINED, POLYMER4 reports
- RTS M40 SE020In2Bones USA, LLC · Prosthesis, Toe, Constrained, Polymer3 reports
- SWANSON G4260102Wright Medical Technology, Inc. · PROSTHESIS, TOE, CONSTRAINED, POLYMER2 reports
- RTS M40 SE030In2Bones USA, LLC · Prosthesis, Toe, Constrained, Polymer1 report
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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