United StatesThe BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742, UDI-DI 00815381020529, Part Number 423742 (Pouch Lot 3VLB25, Kit Lot 1872125; 2,370 pouches / 79 kits) is affected. It was recalled because of an increase in false negative results and was distributed nationwide in AL, AR, IA, IL, KS, LA, MN, MO, TX, and WI.
What's being recalled
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic
Recalling firm: BioFire Diagnostics, LLC, Salt Lake City, UT, United States.
How to identify it
Part Number: 423742 UDI-DI code: 00815381020529 Pouch Lot: 3VLB25 Kit Lot: 1872125
The hazard
Due to increase in false negative results
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
U.S. Nationwide distribution in the states of AL, AR, IA, IL, KS, LA, MN, MO, TX, and WI.
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)