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Vital™ 730M0050Recalls & reported problems

Zimmer Biomet Inc · Class 1

All models of Vital (4)

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 00887868266577), received between Feb 2, 2021 and Feb 2, 2021 — classified as 1 malfunction.

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

  • Fracture1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionFeb 2, 2021Fracture; Fracture

    IT WAS REPORTED THAT A CLOSURE TOP STARTER FRACTURED INTRA-OP. A DIFFERENT DRIVER WAS USED TO COMPLETE THE CASE WITHOUT PATIENT IMPACTS.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 11268046 ↗

Other Screwdriver devices

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Sources and updates

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