FDAClass IIDecember 6, 2017

ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure recall

ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous…

Why was ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure recalled?

There is a possibility that the finished good kits may contain 5 Fr peel-away sheaths instead of the required 4 Fr peel-away sheaths.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot/Batch Number: 23F16M0263

Product
ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous…
Recalling firm
Arrow International Inc
Quantity
N/A
Distribution
Nationwide Distribution to AZ, CA, MA, MO, NC, NY, OR & SD
Recall date
December 6, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls