42 results
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11ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 m
FDA Recall
Open, Classified
·CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel·Product code QWU·August 18, 2025
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX only
FDA Recall
Open, Classified
·CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel·Product code QWU·October 16, 2024
EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202
FDA Recall
Open, Classified
·CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel·Product code QWU·August 18, 2025
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screws accurately, during open or percutaneous computer-assisted spinal surgery.
FDA Recall
Open, Classified
·Augmedics Ltd. 2 Ha-Otsma St Yokneam Illit Northern Israel·Product code OLO·April 14, 2025
DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
FDA Recall
Open, Classified
·Philips North America Llc·Product code JAA·September 21, 2023
DigitalDiagnost C90 High Performance, used to acquire, process, store, display and export digital radiographic images.
FDA Recall
Open, Classified
·Philips North America Llc·Product code JAA·September 21, 2023
ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000
FDA Recall
Open, Classified
·Siemens Medical Solutions USA, Inc·Product code JAA·September 20, 2022
CombiDiagnost R90 R.1.0
FDA Recall
Open, Classified
·Philips North America·Product code JAA·March 3, 2023
CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system
FDA Recall
Open, Classified
·Philips North America Llc·Product code JAA·September 21, 2023
CombiDiagnost R90; Model Number: 709031;
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025
ProxiDiagnost N90. radiography and fluoroscopy system
FDA Recall
Open, Classified
·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany·Product code JAA·May 19, 2021
Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000
FDA Recall
Open, Classified
·Siemens Medical Solutions USA, Inc·Product code JAA·June 10, 2022
AXIOM Luminos Agile
FDA Recall
Open, Classified
·Siemens Medical Solutions USA, Inc·Product code JAA·December 9, 2022
DigitalDiagnost C90 Release 3, used to acquire, process, store, display and export digital radiographic images.
FDA Recall
Open, Classified
·Philips North America Llc·Product code JAA·September 21, 2023
CombiDiagnost R90 Software Version R1.0 and R1.1
FDA Recall
Open, Classified
·Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany·Product code JAA·July 22, 2020
CombiDiagnost R90 is multi-functional general R/F systems.
FDA Recall
Open, Classified
·Philips Healthcare·Product code JAA·September 22, 2021
ProxiDiagnost N90 R.1.0
FDA Recall
Open, Classified
·Philips North America·Product code JAA·March 3, 2023
CombiDiagnost R90 1.1 (709031)
FDA Recall
Open, Classified
·PHILIPS MEDICAL SYSTEMS·Product code JAA·February 11, 2022
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
FDA Recall
Open, Classified
·Philips North America Llc·Product code JAA·September 21, 2023
Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM
FDA Recall
Open, Classified
·Philips North America·Product code JAA·October 27, 2025