SWANSON 4700001Recalls & reported problems
Wright Medical Technology, Inc. · Class 2 · Implant
- 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 00840420121677), received between May 23, 2024 and May 23, 2024 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Fungal Infection1
- Osteolysis1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 23, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT HAD A SWANSON MCP PIP IMPLANTED IN THEIR FINGER. A FEW MONTHS LATER IT WAS REPORTED THAT THE PATIENT HAS A RARE FUNGAL INFECTION. THE INFECTION IS NOT AT THE WOUND. THE HOSPITAL DOES NOT BELIEVE THE INFECTION IS SURGERY RELATED, AND DOES NOT BELIEVE THE PATIENT WOULD HAVE CONTRACTED IT THROUGH THEIR OWN ACTIONS. THE PATIENT UNDERWENT A REVISION.
Patient problems: Fungal Infection; Osteolysis; Pain
MAUDE report 19384116 ↗
Other PROSTHESIS, FINGER, POLYMER devices
- SWANSON 4700020Wright Medical Technology, Inc. · PROSTHESIS, FINGER, POLYMER1 recall0 reports
- SWANSON 4700002Wright Medical Technology, Inc. · PROSTHESIS, FINGER, POLYMER4 reports
- SWANSON G4700004Wright Medical Technology, Inc. · PROSTHESIS, FINGER, POLYMER2 reports
- SWANSON G4700003Wright Medical Technology, Inc. · PROSTHESIS, FINGER, POLYMER2 reports
- SWANSON G4700006Wright Medical Technology, Inc. · PROSTHESIS, FINGER, POLYMER1 report
- SWANSON 4700010Wright Medical Technology, Inc. · PROSTHESIS, FINGER, POLYMER1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.