AGB+ Multi Lumen Central Venous Catheterization Kit recall
AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018
Why was AGB+ Multi Lumen Central Venous Catheterization Kit 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 numbers: Product Codes CDC-42703-XP1A: 23F16M0507 Product Code CDC-47702-XP1A: 23F17A0533
- Product
- AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018
- 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)