OSTEORAPTOR 72202890Recalls & reported problems
Smith & Nephew, Inc. · OSTEORAPTOR TWIST DRILL 2.45 MM · Class 1
All models of OSTEORAPTOR (8)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885554038750), received between Feb 6, 2019 and May 1, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Break” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break3
Patient problems
- Device Embedded In Tissue or Plaque1
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 1, 2026Break
IT WAS REPORTED THAT DURING A BANKART REPAIR PROCEDURE, 2.5MM FLUTED DRILL BROKE. A SMALL AMOUNT OF BONE WAS SHAVED FROM THE GLENOID FOSSA TO EXTRACT THE METAL FRAGMENT. THE DRILL FRAGMENT WAS REMOVED FROM INSIDE THE PATIENT USING SUCTION. THE PROCEDURE WAS RESUMED, AFTER A NON-SIGNIFICANT DELAY, USING A 1.5MM JUGGERKNOT COMPETITOR DEVICE. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25062280 ↗InjuryMar 6, 2025Break; Break
IT WAS REPORTED THAT, DURING AN ARTHROSCOPY, THE TIP OF THE FLUTED DRILL BROKE. THE DISTAL TIP OF THE DRILL WAS FOUND EMBEDDED IN THE BONE AFTER X-RAYS. BROKEN PIECE COULD NOT BE REMOVED FROM THE BODY. THE PIECE WAS LEFT IN THE PATIENT. SURGERY WAS COMPLETED WITH THE SAME DEVICE. THERE WAS NO SURGICAL DELAY.
Patient problems: Device Embedded In Tissue or Plaque; Foreign Body In Patient
MAUDE report 21540039 ↗MalfunctionFeb 6, 2019Break
IT WAS REPORTED THAT DURING A HIP ARTHROSCOPIC, WHEN THE DRILL PREPARED THE PILOT HOLE, THE DRILL TIP GOT BROKEN IN THE BONE. BACK-UP DEVICE WAS USED TO COMPLETE THE SURGERY. NO DELAY WAS REPORTED. BROKEN PIECES REMAIN IN THE PATIENT'S BONE. ADDITIONAL BONE HOLE WAS REQUIRED TO COMPLETE THE SURGERY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8309846 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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