VWING Vascular Needle Guide 00145Recalls & reported problems
Vital Access Corporation · VWING Vascular Needle Guide 8mm 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 08199260101458), received between Mar 24, 2016 and Mar 24, 2016 — 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
- Reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 24, 2016Adverse Event Without Identified Device or Use Problem
IMPLANTING SURGEON REMOVED A VWING DEVICE DUE TO AN APPARENT ALLERGIC REACTION. NO OVERT COMPLICATIONS IDENTIFIED. THE PATIENT TOLERATED THE PROCEDURE WELL. REPORTING NURSE IDENTIFIED THAT THE PATIENT'S ARM HAS RETURNED TO NORMAL FOLLOWING DEVICE REMOVAL. NO FURTHER SYMPTOMS OF REDNESS OR ITCHING.
Patient problems: Reaction
MAUDE report 5522399 ↗
Other Venous Window Needle Guide devices
- VWING Vascular Needle Guide 00146Vital Access Corporation · Venous Window Needle Guide3 reports
- VWING Vascular Needle Guide 00144Vital 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.