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HomeDRG Instruments Gesellschaft mit beschränkter Haftung › Progesterone, 17 a-Hydroxy- (Neonate) (MW) ELISA

Progesterone, 17 a-Hydroxy- (Neonate) (MW) ELISA

DRG Instruments Gesellschaft mit beschränkter Haftung · Model EIA-1429 · UDI-DI 04048474014297

JLX Prescription
10
510(k) clearances
7
Adverse events
3
Recalls
22
Facilities

Description

The quantitative determination of 17-hydroxyprogesterone concentration in human whole blood by a microplate enzyme immunoassay, colorimetric.

Recalls

DateFirmReason
2024-09-13DRG International, Inc.The High and Low Control acceptance ranges in the Certificate of Analysis (CofA) did not match the acceptance range information on the High and Low Control Component labels. Due to
2023-04-05Siemens Healthcare Diagnostics, Inc.Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA Chemistry ToxAmmonia Calibrators for the Atellica CH Salicylate (Sal) Assay due to a positive bias
2023-04-05Siemens Healthcare Diagnostics, Inc.Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA Chemistry ToxAmmonia Calibrators for the Atellica CH Salicylate (Sal) Assay due to a positive bias

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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.