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OsteoMed 330-2008Recalls & reported problems

Osteomed LLC · 2.0mm x 8mm Fully Threaded Screw, Angled Locking · 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 00845694023528), received between Aug 28, 2018 and Aug 28, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

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.

  • MalfunctionAug 28, 2018Insufficient Device Problem Information

    ON (B)(4) 2018, OSTEOMED WAS NOTIFIED OF AN ADVERSE EVENT RELATED TO A PATIENT. PER THE INFORMATION RECEIVED, THE PATIENT RECEIVED IMPLANTS ON (B)(6) 2017. THE IMPLANTS WERE REMOVED ON (B)(6) 2018. NO ADDITIONAL INFORMATION WAS RECEIVED.

    Patient problems: No Information

    MAUDE report 7823991 ↗

Other Screw, fixation, bone devices

All Screw, fixation, bone devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.