FDAClass IIOctober 2, 2019

Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous recall

Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are…

Why was Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous recalled?

Products may contain the incorrect banner card within the kit

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: 13F18H0499

Product
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are…
Recalling firm
Arrow International Inc
Quantity
231 units
Distribution
US Nationwide distribution.
Recall date
October 2, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls