Class II — Luminex Corporation
| Recalling firm | Luminex Corporation |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Two of three complaints were initiated due to the customers repeatedly obtaining No Call results on the Processor SPs in question. |
| Product | Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R |
| Quantity | 4 units |
| Distribution | US: TX, CT, LA |
| Initiated | 2019-04-22 |
| Classified | 2022-04-13 |
| Recall number | Z-0920-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Luminex Corporation (Z-0920-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89051/
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