249 results
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17ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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HLS/HIT Set Advanced with Bioline and/or Softline Coating Console Product Usage: HLS/HIT Set Advanced: The CARDIO HELP System in configuration with the HLS/HIT Set Advanced is intended to be used within the hospital environment and outside the hospital environment (for periods up to six hours), e.g. for intra- and inter-hospital transport. Due to its system combination of integrated oxygenator and centrifugal pump, the HLS Set Advanced is suitable for both extracorporeal pulmonary support and cardiovascular support, and for simultaneous cardiovascular and pulmonary support.
FDA Recall
Terminated
·Maquet Cardiovascular Us Sales, Llc·Product code DTQ·March 5, 2015
ARIA Radiation Oncology, versions 10, 11 , 13.0 and 13.5 with Clinical Assessment License. Model number HIT Product Usage: ARIA Radiation Oncology is a radiation treatment plan and image management application.
FDA Recall
Terminated
·Varian Medical Systems, Inc.·Product code MUJ·September 28, 2015
ImagePilot, Model No. D9MA
FDA Recall
Terminated
·Konica Minolta Medical Imaging USA, Inc.·Product code LLZ·May 9, 2018
CS-7, Model No. A4C1
FDA Recall
Terminated
·Konica Minolta Medical Imaging USA, Inc.·Product code MQB·May 9, 2018
Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision and FLUOROspeed Systems The ceiling type x-ray tube support CH-200 is used to hold the X-ray tube and collimator to position the X-ray tube unit. This unit is used for radiographic examinations of whole body except mammography when combined with an X-ray high voltage generator, an X-ray tube unit, an X-ray collimator, and if necessary, an X-ray radiography stand, an X-ray radiography table, and digital radiography system.
FDA Recall
Open, Classified
·SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku·Product code IYB·October 16, 2025
Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA.
FDA Recall
Open, Classified
·Diagnostica Stago, Inc.·Product code LCO·December 15, 2025
Thoravision II Thorax and Mass Chest Column. Part numbers 4512 130 07812.
FDA Recall
Terminated
·Philips Medical Systems Sales & Service Region No. America·Product code KPR·December 1, 2004
Thoravision I Thorax and Mass Chest Column. Part numbers 4512 130 07811
FDA Recall
Terminated
·Philips Medical Systems Sales & Service Region No. America·Product code KPR·December 1, 2004
Varian brand ARIA Radiation Oncology, ARIA Oncology Information System Radiation Oncology, Import Export Application, Model Number: HIT, Affected Versions: ARIA version 11.0 below 11.0.55, Build 11.0.28 and 11.0.34, Reference/FSCA Identifier: CP-09798; Product is manufactured and distributed by Varian Medical Systems Inc., Palo Alto, CA
FDA Recall
Terminated
·Varian Medical Systems, Inc. Oncology Systems·Product code IYE·November 5, 2012
Storz Documentation Cart with Articulating Arm, Model Number 9601F
FDA Recall
Terminated
·Karl Storz Endoscopy America Inc 600 Corporate Pointe·Product code KOG·March 10, 2006
GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT750HD. Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission.
FDA Recall
Terminated
·GE Healthcare, LLC·Product code JAK·July 25, 2011
GE Signa Ovation 0.35 T MR System. The Signa Ovation System is an open, whole body scanner designed to support improved higher resolution imaging and shorter scan times.
FDA Recall
Terminated
·GE Medical Systems, LLC·Product code LNH·April 16, 2009
GE Signa OpenSpeed 0.7T MR System. The 0.7T Signa OpenSpeed with Excite Magnetic Resonance System is an open, whole body scanner designed to support improved higher resolution imaging and shorter scan times.
FDA Recall
Terminated
·GE Medical Systems, LLC·Product code LNH·April 16, 2009
Varis, Aria Radiation Oncology - Version 8.1.15, 8.5.11, and 8.6.07, Model number HIT-INFSYS, Manufactured by Varian Medical Systems Inc., Palo Alto, CA The Varis RV function is designed to assist the operator of a radiation therapy device in providing accurate treatment setups for each patient by monitoring set up parameters and preventing the radiation therapy device from commencing irradiation while any parameter is out of conformance with the treatment plan. Additional applications provide various data management and library functions.
FDA Recall
Terminated
·Varian Medical Systems Oncology Systems·Product code IYE·May 8, 2009
Hologic Panther(R) Fusion(TM), Catalog number ASY-09600 Product Usage: The Panther instrument is a fully automated sample-to-result instrument, eliminating the need for batch processing and automates all aspects of nucleic acid testing on a single, integrated platform. The Panther can be test samples with random access or batch managed; can perform multiple assays on the same patient sample with up to 4 different assays simultaneously.
FDA Recall
Terminated
·Hologic, Inc·Product code NSU·January 20, 2018
MEVION S250 for Proton Radiation Therapy
FDA Recall
Terminated
·Mevion Medical Systems, Inc.·Product code LHN·March 15, 2016
Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
FDA Recall
Open, Classified
·NRT X-RAY A/S Birkegardsvej 16 Hasselager Denmark·Product code OWB·April 17, 2024
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
AXIOM ARISTOS FX; Multipurpose Radiography System (MPRS) is a dedicated x-ray system with a flat panel detector which allows the acquisition of x-ray exposures without the use of conventional film/screen systems. The MPRS allows radiographic exposures of the whole body including skull, spinal column, chest, abdomen, extremities, and excluding mammography. Radiographic exposures may be taken with the patient in the sitting, standing, or supine positions. The intended use and indications for use of this modified device as described in its labeling have not changed from its predicate device.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code KPR·April 14, 2015
Varian brand Varian ARIA Oncology Information System, Import Export application, v 11.0; Reference/FSCA Identifier: CP-08847; Model Number: HIT; Product is manufactured and distributed by Varian Medical Systems Inc., Palo Alto, CA The ARIA Radiation Oncology product is a treatment plan and image management application. It enables the authorized user to enter, access, modify, store and archive treatment plan and image data from diagnostic studies, treatment planning, simulation, plan verification and treatment. ARIA Radiation Oncology also stores the treatment histories including dose delivered to defined sites and provides tools to verify performed treatments. ARIA also includes optional tools to manage the oncology department's clinical and business information.
FDA Recall
Terminated
·Varian Medical Systems, Inc. Oncology Systems·Product code IYE·July 2, 2012