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JETi WV062FRecalls & reported problems

Walk Vascular L.L.C. · Peripheral Catheter - 6 Fr · 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 B139WV062F0), received between Sep 24, 2022 and Sep 24, 2022 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

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

  • InjurySep 24, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    AFTER A SUCCESSFUL THROMBECTOMY PROCEDURE IN THE LOWER LEFT AND RIGHT EXTREMITIES, THE HEMOGLOBIN DROPPED FROM 9 TO 7 G/DL AFTER THE PROCEDURE AND THE PHYSICIAN ORDERED A BLOOD TRANSFUSION.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 15481531 ↗

Other Aspiration Thrombectomy Catheter devices

All Aspiration Thrombectomy Catheter devices →

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