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Vital™ 850M3000Recalls & reported problems

Zimmer Biomet Inc · Vital™ MIS P.A.T. Tap Stylus · 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 00887868309816), received between Mar 26, 2021 and Mar 26, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inadequate User Interface” (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

  • Inadequate User Interface1

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 26, 2021Inadequate User Interface; Inadequate User Interface

    IT WAS REPORTED THAT A TAP DID NOT PROVIDE TACTILE FEEDBACK FOR THE SURGEON TO GAUGE DEPTH WITH DURING SURGERY. HOWEVER, DEVICE EVALUATION BY THE MANUFACTURER FOUND THAT THE TAP WAS FRACTURED. THERE WERE NO PATIENT IMPACTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11577744 ↗

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Sources and updates

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