Recall Register

Qiagen Sciences LLC: FDA recalls

FDA enforcement reports name Qiagen Sciences LLC as the recalling firm in 18 events. The events have 21 product records. The recalls started from 2016 to 2025. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

18 events, newest first.

FDA enforcement events of Qiagen Sciences LLC
InitiatedProduct (first record)TypeClassRecordsStatus
12 Mar 2025Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/aDeviceClass II1Ongoing
3 Jun 2024QIAcube Connect MDx - IVD Instrument designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model/Catalog Number: 900370 Software Version: 1.0.1DeviceClass II1Ongoing
4 Mar 2024EZ2 Connect MDx-IVD Designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model Number: 9003230DeviceClass II1Ongoing
28 Apr 2023QIAstat-Dx Respiratory SARS-CoV-2 Panel multiplexed nucleic acid real-time PCR test, Reference Number 691223DeviceClass II1Ongoing
20 Jul 2022therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721DeviceClass II3Ongoing
25 Feb 2022therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)DeviceClass II2Ongoing
21 Nov 2021QIAcube Connect MDx, Model No. 9003070DeviceClass II1Ongoing
8 Nov 2021QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223DeviceClass II1Terminated
15 Jan 2021SARS-CoV-2 Antigen TestDeviceClass II1Terminated
11 Dec 2020therascreen PIK3CA RGQ PCR Kit (23) US IVD product- aid clinicians in identifying breast cancer patients who may be eligible for treatment with PIQRAY (alpelisib) based on a PIK3CA Mutation Detected result. REF 873121DeviceClass II1Terminated
15 Jul 2020QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative detection and differentiation of nucleic acid from multiple respiratory viral and bacterial organisms, including the SARS-CoV-2 virus, in nasopharyngeal swabs (NPS) eluted in universal transport…DeviceClass II1Terminated
8 Apr 2020therascreen EGFR RGQ PCR Kit (24), Reference Number REF 870121DeviceClass II1Terminated
21 Feb 2020AmniSure ROM Test, Material Nos. FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Distribution, 10 tests/box), FMRT-1-25-CA (Canadian Distribution; 25 tests/box)DeviceClass II1Terminated
28 Jan 2020QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time detection of PCR assays.DeviceClass II1Terminated
2 Jul 2019QIAsymphony SP SOW 5.0.3, software used with the QIAsymphony SP Instrument (The QIAsymphony SP instrument is designed to perform automated purification of nucleic acids-IVD) Model Number: 9001297 Product Usage: The QIAsymphony SP instrument is designed to perform automated purification of nucleic acids. It is…DeviceClass II1Ongoing
5 Jun 2019Filter-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 preparationDeviceClass I1Terminated
23 Jul 2018EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform automated isolation and purification of nucleic acids. It is intended to be used only in combination with QIAGEN kits indicated for use with the EZ1 Advanced XL instrument for the applications…DeviceClass II1Terminated
2 Feb 2016QFT TB Antigen Tube. QIAGEN Sciences, LLC. The QuantiFERON TB-Gold is an indirect test for M. tuberculosis infection (including disease)DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Qiagen Sciences LLC: events for each product type
TypeEvents
Device18
Qiagen Sciences LLC: events in each class
ClassEvents
Class II17
Class I1
Share of the events of the firm in Class I
6%
Share of all events on the register in Class I
18%
Events with the status Ongoing
8

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Qiagen Sciences LLC, by the year that the recall started. The largest year is 2020, with 5 events.

Official channels

Cite this page

Recall Register. Qiagen Sciences LLC: FDA recalls. https://recallregister.com/firm/qiagen-sciences-llc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
MD

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Qiagen Sciences LLC have?
Class II: 17 events. Class I: 1 event. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Qiagen Sciences LLC?
FDA event 96521, which the firm started on 12 Mar 2025. The first product in the record is: Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/a
How many FDA recalls of Qiagen Sciences LLC have the status Ongoing?
8 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.