FDA Device Intelligence
Home › RICHARD-ALLAN SCIENTIFIC COMPANY › Epredia

Epredia

RICHARD-ALLAN SCIENTIFIC COMPANY · Model Fast Flex™ Holding Solution 5 L · UDI-DI 00673693556064

PPM
10
510(k) clearances
316
Adverse events (1 deaths)
30
Recalls
261
Facilities

Description

The Fast Flex Tissue Processing System was designed to accommodate a wide range of tissue processing demands. These reagents, when used together with the STP 420ES or Pathcentre tissue processors, will significantly reduce tissue processing times and produce very high-quality results. The Fast Flex Tissue Processing System provides optimal tissue processing and staining results based on the patented rotational technology in the main chamber of the STP 420ES and the chemically enhanced Fast Flex reagents. The Fast Flex Tissue Processing System also produces excellent tissue and staining results when used with the Pathcentre tissue processor. Tissue/chemical interactions, reactions, and diffusion rates are accelerated, and depending upon tissue thickness, fatty tissue such as breast, bowel, and lymph node process very efficiently within this system. Our experience has additionally shown that bloody tissues also process well, especially when Holding Solution is utilized in the grossing room. Traditional hematoxylin and eosin staining demonstrates well-delineated nuclear chromatin, as well as superb cytoplasmic contrast.

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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.