SmartSite Extension Set recall
SmartSite Extension Set, Model No. 20029E. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or…
Why was SmartSite Extension Set recalled?
CareFusion is recalling the SmartSite Extension Set due to disconnection and leakage issues.
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 No. 15015769, 15035412, 15045950.
- Product
- SmartSite Extension Set, Model No. 20029E. Used to administer fluid and medications through a needle or catheter inserted into the patient's artery or…
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 21,000 units
- Distribution
- Distributed US (nationwide) and in Canada.
- Recall date
- November 11, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)