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FDAFDA · Food and drugs·Recall number Z-2283-2017

Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters (PICCs) to the goal location which is to the cavo-atrial junction near the sino-atrial node

Published June 14, 2017 · Recall initiated: March 20, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Arrow International Inc
Distributor
Nationwide Distribution
Lot
Material number ASK-04001-DU8
Risk classification
Class II
Area (FDA)
device
Country
United States

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