ILIZAROV 102907Recalls & reported problems
Smith & Nephew, Inc. · WRENCH 10MM WITH FLEXIBLE SOCKET HEAD · Class 1
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 03596010031815), received between Dec 29, 2020 and Dec 29, 2020 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Corroded” (6 reports).
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
- Corroded6
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 29, 2020Corroded; Corroded
IT WAS REPORTED THAT SIX WRENCH 10MM FLEX HEAD ARE RUST AND THE STERILE CENTER REFUSES TO WASH THEM. NO CASE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11093086 ↗MalfunctionDec 29, 2020Corroded; Corroded
IT WAS REPORTED THAT SIX WRENCH 10MM FLEX HEAD ARE RUST AND THE STERILE CENTER REFUSES TO WASH THEM. NO CASE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11092991 ↗MalfunctionDec 29, 2020Corroded; Corroded
IT WAS REPORTED THAT SIX WRENCH 10MM FLEX HEAD ARE RUST AND THE STERILE CENTER REFUSES TO WASH THEM. NO CASE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11092899 ↗MalfunctionDec 29, 2020Corroded; Corroded
IT WAS REPORTED THAT SIX WRENCH 10MM FLEX HEAD ARE RUST AND THE STERILE CENTER REFUSES TO WASH THEM. NO CASE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11092866 ↗MalfunctionDec 29, 2020Corroded; Corroded
IT WAS REPORTED THAT SIX WRENCH 10MM FLEX HEAD ARE RUST AND THE STERILE CENTER REFUSES TO WASH THEM. NO CASE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11091896 ↗MalfunctionDec 29, 2020Corroded; Corroded
IT WAS REPORTED THAT SIX WRENCH 10MM FLEX HEAD ARE RUST AND THE STERILE CENTER REFUSES TO WASH THEM. NO CASE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11091883 ↗
Other WRENCH devices
- MONARCH 277040510Medos International Sàrl · WRENCH199 reports
- PINNACLE 2217-50-008Depuy (Ireland) · WRENCH108 reports
- SIGMA 96-1673Depuy (Ireland) · WRENCH102 reports
- P.F.C. 86-5189Depuy (Ireland) · WRENCH92 reports
- Veptr 03.641.004Synthes GmbH · WRENCH86 reports
- RECLAIM 2975-00-300Depuy (Ireland) · WRENCH51 reports
- PINNACLE 2217-50-006Depuy (Ireland) · WRENCH34 reports
- NA 388.261Synthes GmbH · WRENCH32 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.