FDA recall record

Arrow International Cather, Ultrasound, Intravascular The VPS Stylet and Console are recall — FDA Z-2772-2016

Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.

Class IIclassification
Z-2772-2016official record ID
Sep 21, 2016report date

Recall record at a glance

Official recordZ-2772-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmArrow International Inc.
Report dateSep 21, 2016
Recall initiation dateFeb 17, 2016
Quantity6,121 units in total
LocationReading, PA, United States

Official product description

Cather, Ultrasound, Intravascular The VPS Stylet and Console are indicated for guidance and tip positioning for central venous catheters.

Why the product was recalled

Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.

Distribution information

US Distribution to states of: NC, OH, FL, and MD.

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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