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CHORUS SANITIZING SOLUTION
DIESSE DIAGNOSTICA SENESE SPA · Model 83604 · UDI-DI 08033891328849
PPM
Prescription
10
510(k) clearances
315
Adverse events (1 deaths)
30
Recalls
259
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-26 | Immuno-Mycologics, Inc | Neutralization Buffer may contain contaminants |
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2025-10-29 | Copan Italia | Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed. |
| 2025-10-29 | Copan Italia | Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed. |
| 2025-05-21 | Diagnostica Stago, Inc. | Potential for shorter clotting times in clotting tests which have a dilution, leading to possible overestimate of around 1% |
| 2025-04-24 | Mckesson Medical-Surgical Inc. Corporate Office | transit 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 |
| 2024-09-25 | Biocare Medical, LLC | Kits 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 |
| 2024-05-21 | Ortho-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 |
| 2024-02-07 | Beckman 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 |
| 2023-05-24 | NeuMoDx Molecular Inc | Top 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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Get your free API keyRead the docsData 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.