Siemens Healthcare Diagnostics, Inc Recall: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay ,
Siemens Healthcare Diagnostics, Inc Recall: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay , is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Siemens Healthcare Diagnostics, Inc; Product: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay , 200 ReadyPack Reference Number 10492493 Product Usage:
| Recalling firm | Siemens Healthcare Diagnostics, Inc |
|---|---|
| Product | Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay , 200 ReadyPack Reference Number 10492493 Product Usage: The ADVIA Centaur Syphilis (SYPH) assay is an in vitro diagnostic immunoassay for the qualitative determination of antibodies to Treponema pallidum in human serum or plasma (EDTA, lithium or sodium heparinized, citrate) using the ADVIA Centaur and ADVIA Centaur XP systems as an aid in the diagnosis of syphilis |
| Reason for recall | Syphilis Assay Interference with HBsAg Assay |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution - US Nationwide and the countries of: Foreign: Brazil, China, Denmark, Hong Kong, Malaysia, and New Zealand Viet Nam |
| Recall initiated | 20120717 |
| Recall number | Z-2228-2012 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
Try RecallGuard →