Search Results for: recall

The FDA resent information regarding the October 15, 2012 voluntary field corrective action for the field upgrade kit for GE Healthcare’s resuscitation systems with blender, installed in GE Giraffe and Panda infant warmers.

In the Enforcement Report for the week of January 23 the FDA lists the voluntary Class II Recall by Philips Medical Systems (Cleveland) Inc of the computed tomography x-ray system Brilliance workspace portal.

Stryker Medical Division of Stryker Corp continues its Class II Recall of its medical surgical bed, model numbers 3002S3EX and 3005S3EX.

In the Enforcement Report for the week of January 2, 2013, the FDA listed the Class II recall of the Extended Brilliance workspace (EBW) in order to update the system.

The FDA notified health care professionals that the Fisher & Paykel Healthcare reusable breathing circuit, model 900MR068, was recalled due to pinholes in the tubes used in the reusable breathing circuit.