FDAFDA · Food and drugs·Recall number Z-2700-2017
Alaris Pump Module model 8100
Published July 19, 2017 · Recall initiated: June 12, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CareFusion 303, Inc.
- Distributor
- US and Canada
- Lot
- Notification will be distributed to all Alaris Pumps customers with pumps manufactured between June 2002 through June 2004.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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