# FDA recall Z-2088-2019

> **Qiagen Sciences LLC** · Class I · device recall initiated 2019-06-05.

## Product

Filter-Tips, 1500 ul  (1024 tips/kitbox),  REF 997024- REF: 997024 IVD: Used with the QIAGEN QIAsymphony SP/AS Instruments (REF 9001297 and 9001301) REF: 997024       Used in sample preparation

## Reason for recall

Kit lots contain a small percentage of damaged Filter-Tips that are leaking when being used with the QIAsymphony SP/AS Instruments (REF 9001297 and 9001301)

## Distribution

US Nationwide distribution

## Key facts

- **Recall number:** Z-2088-2019
- **Recalling firm:** Qiagen Sciences LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-05
- **Report date:** 2019-08-07
- **Termination date:** 2020-08-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Germantown, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2088-2019

## Citation

> AI Analytics. FDA recall Z-2088-2019. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-2088-2019. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
