International Medical Devices Database

Manufacturer Address
Quidel Corporation, 10165 Mckellar Ct, San Diego CA 92121-4201
Manufacturer Parent Company (2017)
Quantimetrix Corporation
Source
USFDA
2 Events
- Recall of Device Recall QuickVue OneStep hCG Urine
- Recall of Device Recall Sofia Influenza A B FIA, Kit 20218

2 devices in the database

Device Recall QuickVue OneStep hCG Urine

Model / Serial
Lot Number: 706842
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA including AL, AZ, CA, CO, CT, FL, GA, HI, IL, KS, KY, MA, MD, MN, NC, NJ, NM, NV, OK, OR, PA, TN, TX, UT, VA, and WA and Canada.
Product Description
QuickVue One-Step hCG Urine, Quidel Catalog Number: 20109, Lot Number: 706842

Device Recall Sofia Influenza A B FIA, Kit 20218

Model / Serial
Lot # Range: 208228-214385, 707916-708108 (29 lots).
Product Classification
Immunology and Microbiology Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution - USA (nationwide) and internationally to Korea, Norway, Germany, Chile, Hong Kong, Switzerland, Netherlands, Thailand, Japan, China, and the UK
Product Description
Quidel, Sofia Influenza A + B FIA, Kit #20218 (25-Test Kit), in vitro diagnostic.

11 manufacturers with a similar name

Learn more about the data here

QUIDEL CORPORATION

Manufacturer Parent Company (2017)
Quidel Corporation
Source
MSHM

Quidel Corporation

Manufacturer Parent Company (2017)
Quidel Corporation
Source
LAANSM

Quidel Corporation

Manufacturer Address
Quidel Corporation, 10165 McKellar Ct, San Diego CA 92121-4201
Manufacturer Parent Company (2017)
Quidel Corporation
Source
USFDA

Quidel Corporation

Manufacturer Parent Company (2017)
Quidel Corporation
Source
AEMPSVFOI

Quidel Corporation

Manufacturer Parent Company (2017)
Quidel Corporation
Source
BAM

6 more

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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