Drills DRILL-1.8/100C SRecalls & reported problems

Trimed, INC. · Drill 1.8, 100mm Cannulated Smooth · Class 1

Data updated Oct 18, 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 00842188123870), received between Dec 1, 2023 and Dec 1, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Handling 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Device Handling 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.

MalfunctionDec 1, 2023Device Handling Problem; Device Handling Problem
THE REGIONAL SALES MANGER REPORTED ON 16NOV2023 THAT A SURGEON REPORTS HE HAD A 4TH METACARPAL CASE WHERE HE WAS USING THE DRILL-1.8/100 C S BY HAND AND WAS NOT GETTING ADVANCEMENT, SO HE THEN PUT THE DRILL ON POWER. ONCE ADVANCED ON POWER, THE DRILL BROKE IN 2 AREAS. DRILLS ARE INTENDED TO BE USED UNDER POWER. THE SURGEONH HAD TO RETRIEVE THE PIECES, WHICH CREATED A 30 MINUTE DELAY IN SURGERY. WHEN HE OPENED THE PATIENT FURTHER TO GET THE BROKEN DRILL, HE THEN NOTICED A RUPTURED EXTENSOR TENDON BUT HE DID NOT BELIEVE THAT THE DRILL CAUSED THE TENDON RUPTURE. NO ADDITIONAL HARM WAS CAUSED BY THE DRILL BREAKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18248956 ↗

Device details

UDI-DI	`00842188123870`
Brand	Drills
Model	DRILL-1.8/100C S
Company	Trimed, INC.
Product code	HTW · BIT, DRILL
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Aug 15, 2024

Device type (GMDN): Cannulated surgical drill bit, single-use

A metal shaft intended to be mounted into an appropriate surgical power tool (e.g., a pneumatic reamer or drilling system handpiece with appropriate torque capacity) and rotated to bore into hard/tough tissues (e.g., bone, cartilage) in order to clear a channel of the same diameter as the shaft, typically for the insertion of a prosthetic device or other orthopaedic implant. It has a hollow centre so it can be fed over a drill guiding pin, and may be flexible; devices to assist the procedure (e.g., drill guiding pin, manual driver) may be included. This is a single-use device.

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All BIT, DRILL devices →

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 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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