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Genedrive(R) 96 SARS CoV2 kit

GENEDRIVE DIAGNOSTICS LTD · Model 1 · UDI-DI 05060654860103

QLT Prescription
0
510(k) clearances
1,693
Adverse events
11
Recalls
9
Facilities

Description

Intended to be used for the qualitative detection of RNA from SARS-CoV-2 Low profile 96 well PCR plated assay and optical film for use on Biorad CFX96 instrument.

Recalls

DateFirmReason
2024-09-05Luminex Molecular Diagnostics IncRespiratory pathogen panel may report an elevated rate (7.6% predicted probability of occurrence) of non-specific hMPV target (human Metapneumovirus) results, risk identified pred
2023-05-19Qiagen GmbHIdentified a decreased performance reliability rate, Run abortions could cause delayed diagnosis since sample testing would have to be repeated
2023-05-19Qiagen GmbHIdentified a decreased performance reliability rate, Run abortions could cause delayed diagnosis since sample testing would have to be repeated
2023-04-28Qiagen Sciences LLCFaulty cartridges in the lot could result in false test results.
2022-12-21Roche Molecular Systems, Inc.The firm received customer complaints regarding false negative Influenza A (Flu A) results and late Flu A Target Ct values. A false negative influenza A result may lead to addition
2022-12-21Roche Molecular Systems, Inc.The firm received customer complaints regarding false negative Influenza A (Flu A) results and late Flu A Target Ct values. A false negative influenza A result may lead to addition
2022-12-21Roche Molecular Systems, Inc.The firm received customer complaints regarding false negative Influenza A (Flu A) results and late Flu A Target Ct values. A false negative influenza A result may lead to addition
2022-05-13NeuMoDx Molecular IncThere is a potential for reduced analytical sensitivity for samples in the 1x - 3x LOD range for Flu A, RSV, and SARS-CoV-2 targets. This may lead to false negative results, allowi
2021-11-08Qiagen Sciences LLCThe firm identified sixteen (16) faulty cartridges in LOT 210209, which contain incorrect primer-probe mixes in the reaction chambers. If an affected cartridge is used, false-negat
2021-08-04Roche Molecular Systems, Inc.Customers have reported an increased number of false positive SARS-CoV-2 results.

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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.