10 results
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19ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Smart CR Digital Computed Radiography System; Model Number: CR-IR346RU
FDA Recall
Terminated
·Fujifilm Medical Systems U.S.A., Inc.·Product code IXW·April 1, 2016
ASPRIRE Cristalle Mammography System (cleared under K212873) installed with the ASPIRE Cristalle Digital Breast Tomosynthesis (DBT) Option (approved under P160031).
FDA Recall
Open, Classified
·FUJIFILM Healthcare Americas Corporation·Product code OTE·June 11, 2025
Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as interface to the FUJIFILM Synapse PACS Software (Server)
FDA Recall
Open, Classified
·Fujifilm Medical Systems U.S.A., Inc.·Product code LLZ·May 22, 2020
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
FDA Recall
Open, Classified
·FUJIFILM Healthcare Americas Corporation·Product code KPR·April 11, 2024
Fujifilm Synapse PACS, Software versions: 4.0.xxx, 4.1.xxx, version 4.2.xxx, version 4.3.xxx Medical imaging and information management system, SYNAPSE allows the archiving and distribution of image information from all modalities
FDA Recall
Terminated
·Fujifilm Medical Systems U.S.A., Inc.·Product code LLZ·September 15, 2016
FDR Visionary Suite, CH-200 Model/Version Numbers: (1) 566-16130-23, (2) 566-16130-31, (3) 566-16130-33
FDA Recall
Open, Classified
·FUJIFILM Healthcare Americas Corporation·Product code KPR·September 15, 2025
FDR Visionary Suite; Model Number: CH-200; Version: (1) 566-16130-23, (2) 566-16130-31, (3)
FDA Recall
Open, Classified
·FUJIFILM Healthcare Americas Corporation·Product code KPR·January 9, 2026
SYNCHRON System(s) Chemistry RF Rheumatoid Factor Part Number 475136 RF reagent, when used in conjunction with SYNCHRON LX System(s), UniCel DxC 600/800 System(s) and SYNCHRON Systems CAL 5 Plus, is intended for quantitative determination of Rheumatoid Factor concentration in human serum or plasma.
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code DHR·June 21, 2010
Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The Synapse Cardiovascular image is a management and reporting system
FDA Recall
Terminated
·Fujifilm Medical Systems U.S.A., Inc.·Product code LLZ·April 30, 2021
Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
FDA Recall
Open, Classified
·FUJIFILM Healthcare Americas Corporation·Product code LLZ·February 11, 2025