North American Diagnostics Recalls Unauthorized SARS-CoV-2 Test Kits

Serious injuries or death may result from the use of these devices. This is a Class I recall, the most serious type of recall.

If your email program has trouble displaying this email, view as a webpage. North American Diagnostics Recalls Oral Rapid SARS-CoV-2 Rapid Antigen Test Kits That Are Not Authorized, Cleared, or Approved by the FDA The U.S. Food and Drug Administration has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries, serious health consequences, or death. Read More Questions? Customers with questions about this recall should contact Elizabeth A. Lashinsky, Manager, at ealash52@gmail.com or call 407-312-7104.

Follow us on Twitter at @FDADeviceInfo Manage Subscriptions  |  Unsubscribe All  |  Help

This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration ·  10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA