Multi-Lumen Central Venous Catheterization Kit recall
Multi-Lumen Central Venous Catheterization Kit
Why was Multi-Lumen Central Venous Catheterization Kit recalled?
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
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?
Catolog No - AK-12703 lot number RF3039028
- Product
- Multi-Lumen Central Venous Catheterization Kit
- Recalling firm
- Arrow International Inc
- Quantity
- 65
- Distribution
- US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.
- Recall date
- October 22, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)