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

GE Healthcare Centricity Enterprise Archive, Enterprise Archive, Centricity PACS, Centricity PACS Server, Workflow Core Services, and Core Services Hub Software

GE Healthcare products may associate imaging data with the wrong patient, potentially leading to misdiagnosis or delayed care.

Moderate risk, FDA, Device defect

1 recall that day

GE Healthcare SIGNA Premier Systems

SIGNA Premier systems, whole-body MR scanners, may have ferrous fittings that could attract and cause injury.

Moderate risk, FDA, Device defect

1 recall that day

GE Healthcare Centricity Universal Viewer Zero Footprint Client

Patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client.

Moderate risk, FDA, Device defect