Arsenal Foot 330-27-001Recalls & reported problems
Trilliant Surgical, LLC · 2.7mm Arsenal Screw Drill Bit · 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 00812926029689), received between Jan 6, 2022 and Jan 6, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Dull, Blunt” (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.
Most reported problems
Device problems
- Dull, Blunt1
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.
MalfunctionJan 6, 2022Dull, Blunt; Dull, Blunt
ON 12/09/2021, DJO F&A SALES REPRESENTATIVE CONTACTED DJO F&A SALES SUPPORT SPECIALIST TO REPORT A COMPLAINT REGARDING A 330-27-001 (2.7MM ARSENAL SCREW DRILL BIT) WHICH MALFUNCTIONED DURING A 1ST MPJ FUSION WITH A DOCTOR AT FACILITY 1. DJO F&A SALES REPRESENTATIVE STATED THAT "THE 330-27-001 HAD DIFFICULTY ADVANCING DOWN. THE 330-27-001 WOULD NOT DRILL DOWN OR CUT TO [THE DOCTORS] SATISFACTION. THE DOCTOR HAD TO USE INCREASED FORCE FOR THE DRILL ENGAGE THE BONE AND DRILL TO DESIRED DEPTH. THE DOCTOR SUBSEQUENTLY HIT HIS OTHER HAND AS THE DRILL HAD SLIPPED WITH THE APPLIED PRESSURE. [THE DOCTOR] WAS ABLE TO COMPLETE THE SURGERY SUCCESSFULLY WITH THE USE OF ANOTHER DRILL." DJO F&A SALES REPRESENTATIVE DID NOT RETAIN THE 330-27-001 AND WILL NOT BE SENDING IT BACK TO CORPORATE FOR FURTHER REVIEW.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13177491 ↗
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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