SWANSON 4700010Recalls & 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 00840420121691), received between Dec 8, 2025 and Dec 8, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 8, 2025Fracture; Fracture
IT WAS REPORTED THAT A WRIGHT MEDICAL FINGER JOINT IMPLANT FRACTURED. PER INTAKE DISCUSSION, THE PATIENT IS SCHEDULED FOR A FOLLOW-UP SURGERY TO ADDRESS THE IMPLANT FAILURE.
Patient problems: Insufficient Information
MAUDE report 23751088 ↗
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 4700001Wright 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.