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Arsenal 87012Recalls & reported problems

Alphatec Spine, Inc. · LOCKING POLYAXIAL REDUCTION SCREWDRIVER · Class 1

All models of Arsenal (18)

Data updated Oct 16, 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 00844856069572), received between Apr 30, 2018 and Apr 30, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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.

Most reported problems

Device problems

  • Component Missing1
  • Structural Problem1

Patient problems

  • No Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 30, 2018Component Missing; Structural Problem

    AN INTERNATIONAL CUSTOMER (JAPAN) REPORTED THAT THERE IS NO HEXALOBE PORTION OF THE SCREWDRIVER. IT CANNOT CONNECT WITH REDUCTION SCREW. THE NONCONFORMITY WAS FOUND DURING RECEIVING INSPECTION.

    Patient problems: No Information

    MAUDE report 7472609 ↗

Other SCREWDRIVER devices

All SCREWDRIVER devices →

Sources and updates

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