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 | There is potential for false positive results. |
| Product | Verigene EP Amplification Reagent Kit Test |
| Quantity | 4579 kits |
| Distribution | Worldwide distribution - US Nationwide distribution and the countries of Austria, France, Greece, Japan, and Turkey. |
| Initiated | 2021-08-03 |
| Classified | 2021-09-10 |
| Recall number | Z-2451-2021 |
| 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-2451-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88423/
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