Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo recall
Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42563 JX1A
Why was Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo 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: 23F17E0686, 23F18H0290
- Product
- Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42563 JX1A
- Recalling firm
- Arrow International Inc
- Quantity
- 191 units
- Distribution
- Nationwide Foreign:
- Recall date
- June 26, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)