[Recalled] Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only. — The recall was initiated because the Alaris PC unit model 8015 has a component… | FDA 2012-05-25
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only. |
|---|---|
| Brand / manufacturer | CareFusion 303, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2076-2012 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 25 May 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from CareFusion 303, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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