FDAClass IIFebruary 28, 2018

Multi Lumen Central Venous Catheterization Kit with recall

Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features, and Maximal Barrier Precautions Features; Product…

Why was Multi Lumen Central Venous Catheterization Kit with recalled?

These finished good kits may contain the incorrect Springwire Guide (SWG).

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 number: 23F17C0757

Product
Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features, and Maximal Barrier Precautions Features; Product…
Recalling firm
Arrow International Inc
Quantity
5,926 total
Distribution
Distribution US Nationwide
Recall date
February 28, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls