HUNTER TR300000Recalls & reported problems
Wright Medical Technology, Inc. · Class 1 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840420128942), received between Jun 20, 2022 and Jun 20, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Inaccurate Information” (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.
Most reported problems
Device problems
- Inaccurate Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 20, 2022Inaccurate Information; Inaccurate Information
IT WAS REPORTED DURING THE PROCEDURE THAT THERE WAS A DISCREPANCY IN THE SIZE OF IMPLANT VS THE SIZE LISTED ON THE BOX.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14749070 ↗
Other SPATULA, ORTHOPEDIC devices
- HUNTER PT400000Wright Medical Technology, Inc. · SPATULA, ORTHOPEDIC1 report
- HUNTER TR400000Wright Medical Technology, Inc. · SPATULA, ORTHOPEDIC1 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 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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