Pressure Injectable Multi Lumen Central Venous recall
Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code…
Why was Pressure Injectable Multi Lumen Central Venous 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 number: 13F17C0400
- Product
- Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code…
- 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)