Drills DRILL-1.8/090Recalls & reported problems
Trimed, INC. · Drill 1.8, 90mm · 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 00842188109492), received between Mar 31, 2023 and Mar 31, 2023 — classified as 1 malfunction.
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.
Most reported problems
Device problems
- No Apparent Adverse Event1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 31, 2023No Apparent Adverse Event; No Apparent Adverse Event
A TRIMED SALES REP REPORTED ON (B)(6) 2023 THAT A DRILL-1.8/090 BROKE INSIDE A PATIENT'S RADIUS. THE SURGEON DECIDED IT WOULD BE BEST TO LEAVE THE BROKEN PIECE OF THE DRILL IN THE PATIENT AND DOES NOT BELIEVE IT WILL CAUSE THE PATIENT ANY ADDITIONAL HARM OR IRRITATION. THE TRIMED SALES REP REPORTED THAT THIS DID NOT CAUSE A DELAY IN SURGERY SINCE IT WAS THE LAST HOLE TO BE DRILLED IN ORDER TO COMPLETE THE PROCEDURE.
Patient problems: Foreign Body In Patient
MAUDE report 16656631 ↗
Other BIT, DRILL devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 reports
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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