Drug recall
ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
FDA recall event 69582 · Class II · Siemens Healthcare Diagnostics, Inc.
Key facts
| Event ID | 69582 |
|---|---|
| Recall numbers | Z-0859-2015, Z-0860-2015 |
| Recalling firm | Siemens Healthcare Diagnostics, Inc. |
| Product type | Devices |
| Products | ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests., ADVIA Centaur XP Immunoassay System (including refurbished) Professional use in a laboratory for in vitro diagnostic tests. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress. |
| Initiation date | Oct 9, 2014 |
| Report date | Dec 31, 2014 |
| Termination date | Mar 16, 2017 |
| City | Tarrytown |
| State | NY |
| Country | United States |
| FEI number | 2432235 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: