FDAClass IIJune 26, 2019

Arrow¿ JACC with Chlorag+ard¿ Technology Jugular recall

Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central Catheter Product Code: CDC 43063 JX1A

Why was Arrow¿ JACC with Chlorag+ard¿ Technology Jugular recalled?

Lidstock states the incorrect expiration date for the product

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?

Batch Code: 23F18A0636

Product
Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central Catheter Product Code: CDC 43063 JX1A
Recalling firm
Arrow International Inc
Quantity
12 units
Distribution
Nationwide Foreign:
Recall date
June 26, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
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