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CareFusion 303, Inc. recalls Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.
Recalled August 1, 2012 · FDA recall Z-2076-2012 · CareFusion 303
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. · FDA Class I
Units
112,912 units total (106,888 units in US)
Sold at
US Nationwide Distribution
Description
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.
Product
Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →