Devices

Device Recall Free betahCG ELISA kit

Model / Serial
Catalog number: BC-1023 RN-33853 03-2010 RN-34496 06-2010 RN-34855 06-2010 RN-36539 12-2010 RN-37461 04-2011 RN-39385 09-2011 RN-40775 03-2012 RN-40776 03-2012 RN-41244 05-2012.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution.
Product Description
Free beta-hCG ELISA kit || BioCheck, Foster City, CA 9440. || Quantitative determination of AFP concentration in human serum.
Manufacturer
BioCheck Inc
1 Event
- Recall of Device Recall Free betahCG ELISA kit

Manufacturer

BioCheck Inc

Manufacturer Address
BioCheck Inc, 323 Vintage Park Dr, Foster City CA 94404-1186
Manufacturer Parent Company (2017)
Origene Technologies Inc
Source
USFDA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

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.

Download the data

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.

Download all (zipped)