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MGB Alert Platinum Master Mix-48 rxn

Elitechgroup Mdx LLC · Model M800599 · UDI-DI 03661540950278

PPM
10
510(k) clearances
315
Adverse events (1 deaths)
30
Recalls
259
Facilities

Description

The MGB Alert Platinum Master Mix is intended for use in the development of laboratory assays which target DNA analytes using real-time PCR. The MGB Alert Platinum Master Mix itself generates no diagnostic information or data.

Recalls

DateFirmReason
2026-03-26Immuno-Mycologics, IncNeutralization Buffer may contain contaminants
2025-11-03GET TESTED INTERNATIONAL ABDistribution without premarket approval/clearance.
2025-10-29Copan ItaliaTreatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
2025-10-29Copan ItaliaTreatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
2025-05-21Diagnostica Stago, Inc.Potential for shorter clotting times in clotting tests which have a dilution, leading to possible overestimate of around 1%
2025-04-24Mckesson Medical-Surgical Inc. Corporate Officetransit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failur
2024-09-25Biocare Medical, LLCKits containing the DAB chromogen buffer, intended for use in either manual or automated Immunohistochemistry (IHC) staining protocols, may produce weak to no staining, which may l
2024-05-21Ortho-Clinical Diagnostics, Inc.VITROS Chemistry Products FS Diluent Pack 3, Lot 01-1645 may cause results to be negatively biased when used to dilute patient samples tested with VITROS Chemistry Products CRP Sli
2024-02-07Beckman Coulter, Inc.On 07 February 2024 Beckman Coulter made the decision to conduct a field action on Access Substrate (81906) lots: 234600, 337984, 338040, 338214, 338229, 338289, 338322, 338333, 33
2023-05-24NeuMoDx Molecular IncTop label on some of the NeuMoDx cartridges within these lots may have been incorrectly applied during the manufacturing process, resulting in encroachment into the PCR region. The

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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.