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Performa® 00884450011256Recalls & reported problems

Merit Medical Systems, Inc. · Class 2

All models of Performa (46)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00884450011256), received between Jan 15, 2020 and Jan 15, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • InjuryJan 15, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    THE ACCOUNT ALLEGES THAT THE DURING A VASCULAR PROCEDURE, THE 4F CATHETER TIP DETACHED WITHIN THE PATIENT. THE PHYSICIAN ACQUIRED RETROGRADE VASCULAR ACCESS AND DURING CATHETER MANIPULATIONS THE CATHETER TIP DETACHED. THE PHYSICIAN USED A VASCULAR SNARE DEVICE TO RETRIEVE THE TIP FROM THE PATIENT WITH NO ADDITIONAL CONSEQUENCES TO REPORT.

    Patient problems: Foreign Body In Patient

    MAUDE report 9594349 ↗

Other CATHETER, INTRAVASCULAR, DIAGNOSTIC devices

All CATHETER, INTRAVASCULAR, DIAGNOSTIC devices →

Sources and updates

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