FDA Device recall Z-2076-2012
Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only
- FDA Device
- Class I
- terminated
- Published 2012-08-01
On 2012-08-01 the FDA classified a Class I recall of Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only by Carefusion 303, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2076-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-05-25 |
| Published | 2012-08-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.
Reason
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.
Identifiers
| code_info | not available |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2076-2012%22
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