Devices

Device Recall MULTIGENT Acetaminophen for use with Architect/Aeroset

Model / Serial
Lot 41928UQ11 {exp 2013-01 -31 )
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Illinois
Product Description
MULTIGENT Acetaminophen for use with Architect/Aeroset || Cat. No. 2K99-20. || Assay is intended for the quantitative determination of acetaminophen in human serum or plasma.
Manufacturer
Sekisui Diagnostics Llc
1 Event
- Recall of Device Recall MULTIGENT Acetaminophen for use with Architect/Aeroset

Manufacturer

Sekisui Diagnostics Llc

Manufacturer Address
Sekisui Diagnostics Llc, 31 New York Ave, Framingham MA 01701-8860
Manufacturer Parent Company (2017)
Sekisui Chemical Co. Ltd.
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)