United StatesBiofire Spotfire Respiratory/Sore Throat Panel REF: 423485, Lot Number 2215125 (UDI 00815381020390), 2400 pouches distributed in MS, TX, MN and VA in the United States. BioFire Diagnostics, LLC recalled the product because the test may result in false negative results and control failures.
What's being recalled
Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
Recalling firm: BioFire Diagnostics, LLC, Salt Lake City, UT, United States.
How to identify it
Lot Number: 2215125/UDI: 00815381020390
The hazard
Respiratory/sore throat panel test may result in false negative results and control failures.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the states of MS, TX MN, VA.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)