Devices

Device Recall Medplus ER Drug Screen Test

Model / Serial
Lot Numbers Affected: 85699 and 85671
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
Unclassified
Implanted device?
No
Distribution
Nationwide (distributors in KS and OR).
Product Description
Medplus ER Drug Screen Test Model #5800KAB packaged as 25 individually pouched devices in a labeled kit box.
Manufacturer
Applied Biotech Inc
1 Event
- Recall of Device Recall Medplus ER Drug Screen Test

Manufacturer

Applied Biotech Inc

Manufacturer Address
Applied Biotech Inc, 10237 Flanders Ct, San Diego CA 92121-2901
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)