HAT-TRICK 72204325Recalls & reported problems
Smith & Nephew, Inc. · HAT-TRICK MTP UNILATERAL PROC PACK · Class 2 · Implant
- 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 00885554034882), received between Nov 2, 2017 and Nov 2, 2017 — classified as 1 malfunction.
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.
Most reported problems
Device problems
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 2, 2017Break
THE SUTURE RETRIEVER FROM THE UNILATERAL KIT BROKE WHEN TRYING TO PULL SUTURES THROUGH. A SECOND KIT WAS OPENED AND THE SAME THING HAPPENED. WE THEN OPENED THE BILATERAL KIT TO PULL OUT THE SUTURE RETRIEVER AND USED IT AND IT WORKED. THIS RECORD IS FOR THE FIRST KIT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6997592 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.