FDAClass IIApril 11, 2018

Large Volume Abdominal Paracentesis Kit recall

Large Volume Abdominal Paracentesis Kit

Why was Large Volume Abdominal Paracentesis Kit recalled?

Product packaging may not be completely sealed.

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?

AK 00376

Product
Large Volume Abdominal Paracentesis Kit
Recalling firm
Arrow International Inc
Quantity
30,577 eaches
Distribution
Nationally
Recall date
April 11, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls