Alaris Pump VersaSafe Infusion Set recall
Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
Why was Alaris Pump VersaSafe Infusion Set recalled?
CareFusion is recalling the Alaris VersaSafe Infusion Set because of separation and/or leakages at the VersaSafe split septum port and tubing may lead to leakage of the administration set.
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. 13085603
- Product
- Alaris Pump VersaSafe Infusion Set, Model No. 2122-0007
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 5,760 units
- Distribution
- Michigan
- Recall date
- March 23, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)