Drug recall
Revogene, Catalog no. 610210. IVD test instrument
FDA recall event 90549 · Class II · Meridian Bioscience Inc
Key facts
| Event ID | 90549 |
|---|---|
| Recall numbers | Z-1479-2022 |
| Recalling firm | Meridian Bioscience Inc |
| Product type | Devices |
| Products | Revogene, Catalog no. 610210. IVD test instrument |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | When a run is aborted, the cooling period protection does not occur and the user is able to open the lid prior to the completion of the cooling period, exposing the user to heated instrument… |
| Initiation date | Jun 22, 2022 |
| Report date | Aug 3, 2022 |
| City | Cincinnati |
| State | OH |
| Country | United States |
| FEI number | 1524213 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: