Ø2.8mm DRILL GUIDE, NON-LOCKING/LOCKING PHP 0318-200Recalls & reported problems
Advanced Orthopaedic Solutions, Inc. · Class 2
- 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 00848665032284), received between Dec 2, 2024 and Dec 2, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 2, 2024Physical Resistance/Sticking; Physical Resistance/Sticking
ON (B)(6) 2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT A 0318-200 DRILL GUIDE AND A 0237-200 CALIBRATED DRILL BECAME STUCK. THIS OCCURRED DURING A PROXIMAL HUMERUS FX CASE.
Patient problems: Insufficient Information
MAUDE report 20820700 ↗
Other Appliance, Fixation, Nail/Blade/Plate Combination, Single Component devices
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- CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 48mm 8124-048Advanced Orthopaedic Solutions, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Single Component6 reports
- CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 38mm 8124-038Advanced Orthopaedic Solutions, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Single Component5 reports
- LCP 241.903Synthes GmbH · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, SINGLE COMPONENT5 reports
- CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 44mm 8124-044Advanced Orthopaedic Solutions, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Single Component5 reports
- NA 202.830Synthes GmbH · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, SINGLE COMPONENT5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.