[Recalled] ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests. — A slight crack of the tubing at the connecting fitting on the reservoir connect… | FDA 2014-10-09
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests. |
|---|---|
| Brand / manufacturer | Siemens Healthcare Diagnostics, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0859-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 09 October 2014 |
| EAN / barcode | 10284980 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress.
This Class II 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
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Siemens Healthcare Diagnostics, 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.