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Dynamis AV D0904072075Recalls & reported problems

Creagh Medical Limited · Dynamis PTA UHP 9mm x 40mm x 75cm · 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 05391525783321), received between Jun 29, 2020 and Jun 29, 2020 — classified as 1 malfunction.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1
  • Material Rupture1
  • Structural Problem1

Patient problems

  • Foreign Body In Patient1
  • 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.

  • MalfunctionJun 29, 2020Material Rupture; Structural Problem; Detachment of Device or Device Component; Material Rupture; Structural Problem; Detachment of Device or Device Component

    FOLLOW UP REPORT FOR CC2020-066-IR; MFR REPORT#: 3005994106-2020-00066.

    Patient problems: Foreign Body In Patient; No Consequences Or Impact To Patient

    MAUDE report 10208556 ↗

Other Catheter, Angioplasty, Peripheral, Transluminal devices

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