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StabiliT® 00884450441459Recalls & reported problems

Merit Medical Systems, Inc. · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884450441459), received between Apr 28, 2021 and Apr 28, 2021 — classified as 1 injury.

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

  • Migration1

Patient problems

  • Extravasation1

Recent adverse event reports

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

  • InjuryApr 28, 2021Migration; Migration

    NO DEVICE FAILURE PRODUCT PROBLEM OR MALFUNCTION TO REPORT.

    Patient problems: Extravasation

    MAUDE report 11742160 ↗

Other CEMENT, BONE, VERTEBROPLASTY devices

All CEMENT, BONE, VERTEBROPLASTY devices →

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