Alaris Pump Module recall
Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent Product Code: FPA. The Pump module is intended for facilities that utilize…
Why was Alaris Pump Module recalled?
The recall was initiated because Carefusion has identified a potential risk associated with the Alaris Pump module model 8100. The pump module door keypad overlay may separate from the keypad assembly
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?
Model 8100; Lot/Serial numbers-various
- Product
- Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent Product Code: FPA. The Pump module is intended for facilities that utilize…
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 43,862 units total (40,780 units in the US)
- Distribution
- Worldwide Distribution-USA (nationwide) and the countries of Australia, European Union, and South Africa.
- Recall date
- August 29, 2012
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)