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Salivary Progesterone ELISA

DRG Instruments Gesellschaft mit beschränkter Haftung · Model SLV-2931 · UDI-DI 04048474029314

JLS Prescription
10
510(k) clearances
152
Adverse events
21
Recalls
47
Facilities

Description

Enzyme immunoassay for the in vitro diagnostic quantitative measurement of active free progesterone (a female hormone) in saliva.

Recalls

DateFirmReason
2022-11-09Biomerieux IncAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
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
2019-07-10Siemens Healthcare Diagnostics, Inc.There is a potential for low discordant progesterone results on a subset of patient samples. A falsely low progesterone result may lead to the consideration for additional progest
2019-07-10Siemens Healthcare Diagnostics, Inc.There is a potential for low discordant progesterone results on a subset of patient samples. A falsely low progesterone result may lead to the consideration for additional progest
2019-06-06DRG Instruments GmbHSalivary Progesterone assay may observe a higher percentage of samples with low results. Saliva samples in the low measuring range of the kit {< 20 pg/ml) were assayed and producin
2018-11-21Abbott Ireland Diagnostics DivisionAbbott has become aware of a manufacturing issue that can result in damage to a bottle neck in some of the reagent cartridges found in the lots listed in Appendix A. If a bottle n
2018-03-05Tosoh Bioscience IncAsfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the assay.
2018-02-13Tosoh Bioscience IncFalsely elevated progesterone assay values will occur when using certain progesterone assay part numbers due to cross reactivity of DHEA-S, a metabolite of the DHEA (dehydroepiandr
2018-02-13Tosoh Bioscience IncFalsely elevated progesterone assay values will occur when using certain progesterone assay part numbers due to cross reactivity of DHEA-S, a metabolite of the DHEA (dehydroepiandr
2017-12-22Arrow International IncCertain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.

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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.