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AOS Hex Screw Driver 2.5mm 0432-200Recalls & reported problems

Advanced Orthopaedic Solutions, Inc. · 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 00848665001846), received between Mar 28, 2022 and Mar 28, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

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.

  • MalfunctionMar 28, 2022Break

    ON 3/10/2022 IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN 0432-200 HEX SCREW DRIVER BROKE AT THE TIP WHILE INSERTING A SCREW. ALL WAS RETRIEVED. NO PATIENT AFFECT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13928793 ↗

Other Orthopedic Manual Surgical Instrument devices

All Orthopedic Manual Surgical Instrument devices →

Sources and updates

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