International Medical Devices Database

Manufacturer Address
Inverness Medical Professional Diagnostics, 10 Southgate Rd, Scarborough ME 04074-8303
Source
USFDA
1 Event
- Recall of NOW

One device in the database

NOW

Model / Serial
Lot Number: 024448 Exp. Date: March 14, 2008
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Canada, EU, South Korea, Singapore
Product Description
NOW Legionella Urinary Antigen Test. 22 test kit. For In Vitro Diagnostic Use || Product Code: 852-000

One manufacturer with a similar name

Learn more about the data here

Inverness Medical Professional Diagnostics

Manufacturer Address
Inverness Medical Professional Diagnostics, 2 Research Way, Princeton NJ 08540-6628
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)