DiaSorin Molecular LLC
5 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (5)
Registered facilities (1)
- DiaSorin Molecular LLC FEI 2023365 · CA
Recalls & enforcement
- Class IIOngoing2023-06-14There is a potential for the direct amplification disc to malfunction which may result in spillage of liquid from the disc.
- Class IIOngoing2023-01-30Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays, may leak and cause contamination, cross-contamination, invalid results, and error codes.
- Class IIOngoing2021-11-19A subset of affected discs are at risk of leakage when it is used more than one time with Simplexa COVID-19 Direct and/or Simplexa Flu A/B & RSV Direct Gen II. Leakage from a well that had a positive sample may cause further cross-contamination in areas of the lab if not properly…
- Class IIOngoing2021-09-23Due to unapproved raw materials used in the manufacturing of Covid-19 control pack, their is the potential for delayed amplification signals.
- Class IITerminated2020-05-12Due to a software malfunction in the Multi Assay Suite, there is the probability of increased occurrence of false negative results.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “DiaSorin Molecular LLC — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9089763-diasorin-molecular-llc/
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