Skip to main content

Medical device recalls

Medical device recalls from FDA, newest first. Company page 3 recalls Each recall is dated by the day its recall page names (how recalls are dated).
Agency
Risk level
Status
Date
Sold in

1 recall that day

BioFire FilmArray Pneumonia and Joint Infection Panels

The FilmArray Pneumonia Panel, Pneumonia Panel plus, and BioFire Joint Infection Panel may give false positive results due to contamination.

Moderate risk, FDA, Device defect

1 recall that day

BIOFIRE Respiratory Panel 2.1 (RP2.1)

The Biofire Respiratory Panel 2.1 may give false negative results.

Moderate risk, FDA, Device defect

1 recall that day

Biofire Spotfire Respiratory/Sore Throat Panel

The Biofire Spotfire Respiratory/Sore Throat Panel may result in false negative results and control failures.

Moderate risk, FDA, Device defect