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Estradiol (serum) ELISA

DRG Instruments Gesellschaft mit beschränkter Haftung · Model CLA-4664 · UDI-DI 04048474046649

CHP Prescription
10
510(k) clearances
719
Adverse events (1 deaths)
31
Recalls
55
Facilities

Description

The DRG Estradiol CLIA is a chemiluminescence immunoassay for the quantitative in vitro diagnostic measurement of Estradiol in serum and plasma.

Recalls

DateFirmReason
2022-11-09Biomerieux IncAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
2022-03-03Siemens Healthcare Diagnostics, Inc.Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
2022-03-03Siemens Healthcare Diagnostics, Inc.Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
2022-03-03Siemens Healthcare Diagnostics, Inc.Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
2022-03-03Siemens Healthcare Diagnostics, Inc.Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
2022-03-03Siemens Healthcare Diagnostics, Inc.Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
2022-03-03Siemens Healthcare Diagnostics, Inc.Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
2021-09-22bioMerieux, Inc.bioMerieux has been receiving an increasing number of complaints linked to a VIDAS substrate error. It prevents the test from being run, therefore leads to potential delayed result
2020-02-05Siemens Healthcare Diagnostics, Inc.Due to high discordant Estradiol results which.potentially affects all patient populations, A falsely elevated estradiol level could lead a clinician to misinterpret a patient as p
2020-02-05Siemens Healthcare Diagnostics, Inc.Due to high discordant Estradiol results which.potentially affects all patient populations, A falsely elevated estradiol level could lead a clinician to misinterpret a patient as p

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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.