# FDA recall Z-2596-2018

> **QIAGEN** · Class II · device recall initiated 2018-05-28.

## 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

## Distribution

Domestic - MD  Internationally - AE, AU , CZ, DE, DZ, ES, FR, GB, HK , IE, IT, NO, RO & SA

## Key facts

- **Recall number:** Z-2596-2018
- **Recalling firm:** QIAGEN
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-28
- **Report date:** 2018-08-08
- **Termination date:** 2019-04-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** KOELN, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2596-2018

## Citation

> AI Analytics. FDA recall Z-2596-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2596-2018. Source: US FDA. Licensed CC0.

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