FDA Device Intelligence
Home › Siemens Healthcare Diagnostics Inc. › ADVIA Centaur® H2n

ADVIA Centaur® H2n

Siemens Healthcare Diagnostics Inc. · Model 10308994 · UDI-DI 00630414471235

NCW
1
510(k) clearances
0
Adverse events
1
Recalls
3
Facilities

Description

HER-2/neu - CENTAUR - RGT - 50 tests

Recalls

DateFirmReason
2020-08-25Siemens Healthcare Diagnostics, IncSiemens confirmed that the Upper Limit of Normal (ULN) as claimed in the Instructions for Use (IFU) was no longer achieved. This can potentially result in false positive or false n

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.