Alaris Pump Module recall
Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump…
Why was Alaris Pump Module recalled?
During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion to be interrupted.
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?
All products manufactured or serviced in the time period October 2011 through June 2015.
- Product
- Alaris Pump Module, Model No. 8100 and AIL sensor kits, P/N 147083-102 and P/N 49000221. The Alaris Pump module is a large volume infusion pump…
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 382,635 units
- Distribution
- Nationwide Distribution
- Recall date
- January 25, 2017
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)