VWING Vascular Needle Guide 00144Recalls & reported problems
Vital Access Corporation · VWING Vascular Needle Guide 6mm x 7mm · Class 2 · Implant
- 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 08199260101441), received between Jan 14, 2017 and Jan 14, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Improper Flow or Infusion” (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
- Improper Flow or Infusion1
Patient problems
- Post Operative Wound Infection1
- Skin Inflammation1
- Swelling1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 14, 2017Improper Flow or Infusion
(B)(6) EXPERIENCED A FLOW ISSUE AT OR NEAR A VWING DEVICE IN MID-(B)(6) 2016. FISTULAGRAM SHOWED STENOSIS. SITE WAS ANGIOPLASTIED, AFTER WHICH THE ARM BECAME SWOLLEN AND HOT. (B)(6)'S MENTAL STATUS CHANGED, AND (B)(6) WAS SENT TO THE HOSPITAL. (B)(6) WAS DIAGNOSED WITH A SYSTEMIC INFECTION.
Patient problems: Post Operative Wound Infection; Skin Inflammation; Swelling
MAUDE report 6252149 ↗
Other Venous Window Needle Guide devices
- VWING Vascular Needle Guide 00146Vital Access Corporation · Venous Window Needle Guide3 reports
- VWING Vascular Needle Guide 00145Vital Access Corporation · Venous Window Needle Guide1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.