FDAFDA · Food and drugs·Recall number Z-2076-2012
Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.
Published August 1, 2012 · Recall initiated: May 25, 2012
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
The recall was initiated because the Alaris PC unit model 8015 has a component on the PC unit power supply board that is causing an error code(120.4630) "System Error" or "Missing Battery Error" at start up. The error code is accompanied by both an audible alarm and visual error messages on the PC unit screen.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CareFusion 303, Inc.
- Distributor
- US Nationwide Distribution
- Lot
- not available
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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