SWANSON G4260101Recalls & reported problems
Wright Medical Technology, Inc. · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840420127464), received between Apr 11, 2024 and Apr 11, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
- Degraded1
- Fracture1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 11, 2024Break; Degraded; Fracture; Break; Degraded; Fracture
IT WAS REPORTED THAT THE PATIENT STUBBED THEIR TOE 3 MONTHS POST-OP CAUSING THE IMPLANT TO FAIL, DEGRADING AND BREAKING LATERALLY. THE PATIENT UNDERWENT A REVISION SURGERY 5 MONTHS POST-OP.
Patient problems: Failure of Implant
MAUDE report 19093329 ↗
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 51-108070Biomet Orthopedics, LLC · PROSTHESIS, TOE, CONSTRAINED, POLYMER6 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
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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