Alaris Pump Module recall
Alaris Pump Module model 8100
Why was Alaris Pump Module recalled?
There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.
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?
Notification will be distributed to all Alaris Pumps customers with pumps manufactured between June 2002 through June 2004.
- Product
- Alaris Pump Module model 8100
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 35,940 units
- Distribution
- US and Canada
- Recall date
- July 19, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)