NA 702450Recalls & reported problems
Stryker GmbH · Cannulated Drill · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540112040), received between Sep 26, 2018 and May 1, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Mechanical Jam” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Jam1
- Physical Resistance/Sticking1
Patient problems
- Insufficient Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 1, 2024Mechanical Jam; Mechanical Jam
THE CUSTOMER REPORTED THAT "TAP STUCK IN THE BIT".
Patient problems: Insufficient Information
MAUDE report 19226694 ↗MalfunctionSep 26, 2018Physical Resistance/Sticking
ATTEMPTED TO USE ASNIS 5 MM AND ATTEMPTED TO PASS THE DRILL THROUGH THE GUIDE PIN WHERE THE DRILL STUCK HALFWAY. CONTINUED TO USE IT AS IT WAS, BUT THEN STACKED SEVERAL TIMES AFTERWARDS. A BLACK RELICILE CAME OUT AFTER REMOVING THE POSTOPERATIVE GUIDE PIN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7911790 ↗
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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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