Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Qiagen Sciences LLC

Qiagen Sciences LLC Recalls

All product recalls associated with Qiagen Sciences LLC.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

423

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1881–1900 of 4598 recalls

Qiagen Sciences LLC: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time P...

When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs export, the .csv file reports the calculated concentration result value as a logarithmic value, and could lead to a false negative result, which could lead to serious medical consequences such as the suspension or non-initiation of treatment

FDAJan 28, 2020Nationwide• Qiagen Sciences LLC

Solifenacin Succinate Tablets (Breckenridge) – Manufacturing Deviation (2020)

CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might convert to Solifenacin Tartrate Tablets.

Class IIModerate

FDAJan 24, 2020Nationwide• Breckenridge Pharmaceutical, Inc

Solifenacin Succinate Tablets (Breckenridge) – Manufacturing Deviation (2020)

CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might convert to Solifenacin Tartrate Tablets.

1...93 949596 97...230

Page 95 of 230Next

Class IIModerate

FDAJan 24, 2020Nationwide• Breckenridge Pharmaceutical, Inc

Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany: LN 3R70-01; software version 2.6.2 and earlier. The soft...

Abbott has identified potential performance issues for the Alinity ci -series Software version 2.6.2 and earlier.

FDAJan 24, 2020Nationwide• Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany

St Jude Medical, Cardiac Rhythm Management Division: Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (...

Past updates to programmers and transmitters may lead some implantable cardioverter defibrillators (ICD) to lose wireless radiofrequency (RF) communication; which means patients can no longer be interrogated with wireless RF telemetry or monitored remotely.

FDAJan 22, 2020AZ, CA, DE +16 more• St Jude Medical, Cardiac Rhythm Management Division

BIOMERIEUX Grenoble Biomerieux Institut Christophe Merieux; 5 Rue Des Berges; Cs: NUCLISENS Lysis Buffer, IVD, REF 200292, 48X2 ML LYS Man...

Following a customer complaint about colored eluates, leading to invalid results bioMerieux has confirmed an issue with NUCLISENS Lysis Buffer, ref. 200292, lot 19040201. The issue is linked to drift of pH electrode dysfunction.

FDAJan 10, 2020Nationwide• BIOMERIEUX Grenoble Biomerieux Institut Christophe Merieux; 5 Rue Des Berges; Cs

2020 GENUINE SCOOTER ROYAL ALLOY Recall: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:PADS

Genuine Scooters, LLC. (Genuine Scooters) is recalling certain 2020 Royal Alloy GT150 scooters. The front brake rotor may become uncentered within the front brake caliper allowing the inner brake pad to dislodge from the top of the brake caliper.

NHTSAJan 10, 2020Nationwide• GENUINE SCOOTER

Razzoo's Creole Sauce (National Food) – Undeclared Codfish (2020)

Undeclared Allergen

Undeclared codfish powder

Class IIModerate

FDAJan 6, 2020TX• National Food & Beverage, Inc

Razzoo's Gumbo Base (National Food) – Undeclared Codfish (2020)

Undeclared Allergen

Undeclared codfish powder

Class IIModerate

FDAJan 6, 2020TX• National Food & Beverage, Inc

Razzoo's Etouffee Sauce (National Food) – Undeclared codfish (2020)

Undeclared Allergen

Undeclared codfish powder

Class IIModerate

FDAJan 6, 2020TX• National Food & Beverage, Inc

GE Healthcare, LLC: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System, ...

It was identified that due to a potential installation workflow issue, the MR system date could be set incorrectly. The system s date and time setting are used to populate the DICOM header information on images. This could result is an inaccurate date recorded on the images.

FDADec 23, 2019Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: SIGNA Architect Nuclear Magnetic Resonance Imaging System...

It was identified that due to a potential installation workflow issue, the MR system date could be set incorrectly. The system's date and time setting are used to populate the DICOM header information on images. This could result is an inaccurate date recorded on the images.

FDADec 23, 2019Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: SIGNA Premier Nuclear Magnetic Resonance Imaging System -...

FDADec 23, 2019Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System -...

FDADec 23, 2019Nationwide• GE Healthcare, LLC

Buderus Oil Boilers (Bosch) – Carbon monoxide risk (2019)

This recall involves Buderus brand GB125-35 oil-condensing boilers distributed by Bosch. The boilers have a blue enclosure, and the GB125-35 model number is located on the data plate near the top right hand side of the boiler. The Buderus brand name is printed on the outside of the boiler's blue enclosure. Bosch Thermotechnology and the model number are printed on a white label on the blue enclosure.

CPSCDec 20, 2019Nationwide• Bosch Thermotechnik GmbH, of Germany

Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany: CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030...

When using the Table Up/Down button, the system may experience Error 80, which locks the geometry in that specific state, requiring the intervention of a service Engineer. Additionally, the thermos switch, which handles power down of the unit in case of transformer overheating, was installed incorrectly at production.

FDADec 19, 2019Nationwide• Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany

RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden: RayStation stand-alone software treatment planning system...

Three issues found: i) The Map ROI options in the ROI list in the Structure Definition module may generate unintended ROI geometries ii) Elekta guard leaf behavior. There is an interoperability issue with Elekta regarding setting of guard leaves. iii)SSD, when intended as source-to-surface distance, it sometimes gives source-to-skin distance.To the best of our knowledge, these issues have not caused any patient mistreatment or other incidents. However, the user must be aware of the following information to avoid incorrect dose calculations during treatment planning.

FDADec 19, 2019Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany: CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030...

FDADec 19, 2019Nationwide• Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany

Vitreq Bv Seggelant-Noord 2 Vierpolders Netherlands: VitreQ 25G Blunt Needles with luer-lock connector-REF : ...

Microscopic tears of the sterile pouch may compromise sterility

FDADec 17, 2019Nationwide• Vitreq Bv Seggelant-Noord 2 Vierpolders Netherlands

Vitreq Bv Seggelant-Noord 2 Vierpolders Netherlands: VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423

Microscopic tears of the sterile pouch may compromise sterility

FDADec 17, 2019Nationwide• Vitreq Bv Seggelant-Noord 2 Vierpolders Netherlands