Skip to main content

Medical device recalls

Medical device recalls from FDA, newest first. Company page 2 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

Accriva Diagnostics Hemochron Jr. APTT Test Cuvettes

The Hemochron Jr. APTT test cuvette may have a mispositioned or absent reagent, causing erroneous results and potential thrombosis.

Moderate risk, FDA, Device defect

1 recall that day

DirectCHECK ACT-LR Whole Blood Quality Control, Level 2

The directCHECK ACT-LR whole blood quality control has labeling with an incorrect performance range.

Moderate risk, FDA, Labeling error