FDA (Devices) recall action 95579
The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.
Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.
The agency’s own wording, quoted from the enforcement report.
Philips is recalling Zenition 70 devices because the mains control unit board fuse may blow during start-up or procedures.
Philips Zenition 50 imaging systems may experience mains control unit fuse failure during startup or procedures. The defect could cause equipment malfunction.