JETi WV088FRecalls & reported problems
Walk Vascular L.L.C. · Peripheral Catheter - 8 Fr · Class 2
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 B139WV088F0), received between Aug 26, 2022 and Aug 26, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Fever1
- Low Blood Pressure/ Hypotension1
- Tics/Tremor1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 26, 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 EXTREMITY, THE SUBJECT DEVELOPED AN ACUTE ONSET OF HYPOTENSION, TREMORS, AND FEVER REQUIRING TREATMENT AND PROLONGED HOSPITALIZATION. THE PATIENT WAS TREATED WITH MEDICATION AND THE ADVERSE EVENT WAS RESOLVED THE NEXT DAY ((B)(6) 2022).
Patient problems: Fever; Low Blood Pressure/ Hypotension; Tics/Tremor
MAUDE report 15299549 ↗
Other Aspiration Thrombectomy Catheter devices
- AlphaVac 25-302Angiodynamics, Inc. · Aspiration thrombectomy catheter12 deaths17 reports
- AlphaVac H787253020Angiodynamics, Inc. · Aspiration thrombectomy catheter2 deaths5 reports
- JETi™ WV8803AAbbott Vascular Inc. · Aspiration Thrombectomy Catheter4 reports
- AlphaVac 25-301Angiodynamics, Inc. · Aspiration thrombectomy catheter4 deaths4 reports
- JETi™ WVSDUPAbbott Vascular Inc. · Aspiration Thrombectomy Catheter3 reports
- JETi™ WV6203AAbbott Vascular Inc. · Aspiration Thrombectomy Catheter2 reports
- QuickClear Thrombectomy System AC10SH085Volcano Atheromed, Inc. · Aspiration Thrombectomy Catheter2 reports
- ASAPLP™ 00884450555125Merit Medical Systems, Inc. · Aspiration thrombectomy catheter2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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