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Tools - Screws GUIDEQ-1.8Recalls & reported problems

Trimed, INC. · Quick Guide, 1.8mm · Class 1

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 00842188112898), received between Sep 7, 2021 and Sep 7, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Product Quality Problem” (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

  • Product Quality Problem1

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.

  • MalfunctionSep 7, 2021Product Quality Problem; Product Quality Problem

    A TRIMED SALES REPRESENTATIVE REPORTED ON (B)(6) 2021 THAT THE GUIDEQ-1.8 FROM A WRIST FIXATION SET HAD "NOT FOR HUMAN USE" LASER MARKED ON THE BOTTOM OF THE DRILL GUIDE. HE STATED THIS DEVICE WAS FOUND DURING A ROUTINE CHECK OF HIS TRAY AND THAT HE IS UNSURE IF THE DEVICE HAD COME IN CONTACT WITH A PATIENT BUT DOESN'T BELIEVE THIS ISSUE CAUSED ANY ADDITIONAL PATIENT HARM OR DELAY IN SURGERY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12433457 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.