FDA recall record

Arrow VPS Access Kit with Maximal Barrier Precautions for use with 4 Fr recall — FDA Z-2283-2017

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

Class IIclassification
Z-2283-2017official record ID
Jun 14, 2017report date

Recall record at a glance

Official recordZ-2283-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmArrow International Inc.
Report dateJun 14, 2017
Recall initiation dateMar 20, 2017
Quantityunknown-firm reports total devices distributed 43,394
LocationReading, PA, United States

Official product description

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

Why the product was recalled

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.

Distribution information

Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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