FUJIFILM Healthcare Americas Corporation: Medical Device Recalls in 2024

According to to data from the FDA, there were 11 medical device recalls made by FUJIFILM Healthcare Americas Corporation in 2024. See the details of the recalls below.

You can see similar recalls for other firms.

• The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray detectors coupled.
• FDR Visionary Suite - Intended to generate digital or conventional radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts of human anatomies in all routine radiography examinations. Model/Catalog Number: 566-16130-23 566-16130-33
• Synapse PACS - Version 7.2.100
• Synapse PACS - Version 7.2.200
• Synapse PACS - Version 7.1.000US
• Synapse PACS - Version 7.1.000
• Synapse PACS - Version 7.2.000
• Synapse PACS - Version 7.3.000
• Synapse Cardiology PACS V7.3.0, V7.2, V7.1, V7.0. A web-based application as the primary user interface for the processing of medical images.
• Synapse CV 6. with AR. A web-based application as the primary user interface for the processing of medical images.
• Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24