EZ1 DSP Virus Kit — Class II medical device recall Z-2596-2018
Terminated recall by QIAGEN, reported 2018-08-08. Underfilled reagent well that could lead to incorrect results
| Recall number | Z-2596-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | QIAGEN, KOELN, N/A, Germany |
| Recall initiated | 2018-05-28 |
| Classified | 2018-08-02 |
| Reported by FDA | 2018-08-08 |
| Terminated | 2019-04-05 |
| Quantity | 287 units |
| UPC / GTIN / UDI-DI | 04053228000099 |
| Lot numbers | 160020069 |
| Model numbers | 62724 |
| Expiration dates | 2019-11-01 |
Product
EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use.
Reason for recall
Underfilled reagent well that could lead to incorrect results
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2596-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.