25 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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INFX-8000C XGCP-930AA TABLE SIDE CONSOLE, INFX-8000C XGCP-930BA TABLE SIDE CONSOLE
FDA Recall
Open, Classified
·Canon Medical System, USA, INC.·Product code OWB·June 22, 2023
Toshiba Aquilion ONE CT SystemTSX-301 A/2D
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·February 3, 2009
TSX-101A Aquilion 32/64 ONE Computed Tomography X-Ray System; TXS-101/R Aquilion RXL Computed Tomography X-Ray System; TSX-301A Aquilion One Computed Tomography X-Ray System; TSX-301B Aquilion Premium Computed Tomography X-Ray System; TSX-302A Aquilion Prime Computed Tomography X-Ray System. This device is indicated to acquire and display cross sectional volumes of the whole body, to include the head. The Aquilion RXL has the capability to provide volume sets. These volume sets can be used to perform specialized studies, using indicated software/hardware, by a trained and qualified physician.
FDA Recall
Terminated
·Toshiba American Medical Systems Inc·Product code JAK·October 1, 2013
20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use with PAB(R) Containers, BC2000 Product is intended for fluid transfer between a Partial Additive Bag (PAB(R)) container and a drug vial.
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code LHI·April 4, 2013
13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use with PAB(R) Containers, BC1300 Product is intended for fluid transfer between a Partial Additive Bag (PAB(R)) container and a drug vial.
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code LHI·April 4, 2013
Pursuit ureteral dilation balloon catheters, 6 mm x 4 cm. Order # PAB-050080-6-4.0
FDA Recall
Terminated
·Cook Urological, Inc.·Product code EZN·January 22, 2003
Pursuit ureteral dilation balloon catheters, 6 mm x 8 cm. Order # PAB-050080-6-8.0
FDA Recall
Terminated
·Cook Urological, Inc.·Product code EZN·January 22, 2003
VENTANA anti-Helicobacter Pylori (SP48) PAB 250, Catalog Number 06425623001, model 790-1015 Immunohistochemistry (IHC) for in vitro diagnostic use.
FDA Recall
Terminated
·Ventana Medical Systems Inc·Product code OWF·August 2, 2018
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, with Component PCB, TSI/RSI firmware C29278
FDA Recall
Open, Classified
·Beckman Coulter, Inc.·Product code JJE·February 6, 2025
Replacement LED PCB Kit, part number 001840, of the Natus neoBLUE (aka neoBLUE 2) Phototherapy system. Neonatal phototherapy.
FDA Recall
Terminated
·Natus Medical Incorporated·Product code LBI·November 19, 2014
B. Braun addEASE Binary Connector, Catalogue #N7990, 200 units (50 units per bag with 4 bags per shipping box) Intended for use in a pharmacy setting to connect a B. Braun 250mL Excel IV solution bag to a 20 mm drug vial for reconstituting or mixing the drug in the vial with the solution in the bag.
FDA Recall
Terminated
·B. Braun Medical Inc·Product code LHI·June 24, 2010
B. Braun addEASE Binary Connector, Catalogue #N7993, 200 units (50 units per bag with 4 bags per shipping box) Intended for use in a pharmacy setting to connect a B. Braun 250mL Excel IV solution bag to a 20 mm drug vial for reconstituting or mixing the drug in the vial with the solution in the bag.
FDA Recall
Terminated
·B. Braun Medical Inc·Product code LHI·June 24, 2010
CELL-DYN Sapphire Probe Detector PCB Assembly (also called the Aspiration Bottom Sensor) used on the Cell-Dyn Sapphire Hematology Analyzer, Manufactured by Abbott Laboratories, Santa Clara, CA
FDA Recall
Terminated
·Abbott Laboratories·Product code GKZ·April 5, 2010
Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN 651501684994). Blood convenience kit. The Transfusion Set includes the items necessary to administer the collected blood to a patient.
FDA Recall
Terminated
·Combat Medical Systems, LLC·Product code POQ·December 23, 2020
Integrated Gate Controller PCB (component of AlignRT Plus) Truebeam variant only. The AlignRT is a video-based three-dimensional (3D) surface imaging system which is used to image the skin surface of a patient in 3D before and during radiotherapy treatment. Part number: V000172
FDA Recall
Terminated
·Vision RT Ltd Dove House Arcadia Avenue London United Kingdom·Product code IYE·August 24, 2018
Centurion FCP MAGILL CATH 7.5 IN PED (67575), Product Code 67575
FDA Recall
Open, Classified
·MEDLINE INDUSTRIES, LP Northfield·Product code BWB·February 23, 2024
Sarns 8000 Cardioplegia Monitor, Catalog Number 16414; also known as PROG COMP BD AMPRO 420 CPG 8K, Catalog Number 816373 The Sarns 8000 Cardioplegia Monitor is indicated to measure extracorporeal line pressure and signal when the pressure exceeds the operator-set limit.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corporation·Product code DWB·August 29, 2011
Sony LMD-1951MD, Sony LMD1951MD/BS, Sony LMD-1951MC (Foreign) 19 inch medical grade liquid crystal display (LCD) Medical Monitors with light-emitting diode (LED) backlight technology.
FDA Recall
Terminated
·Sony Medical Systems·Product code FWB·January 13, 2015
Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions for the purpose of archiving and teaching.
FDA Recall
Terminated
·Trumpf Medical Systems, Inc.·Product code FWB·December 15, 2017
Battery Module for Sarns Modular Perfusion System 8000 Product Usage: The Sarns Modular Perfusion System 8000 is indicated for up to 6 hours use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corporation·Product code DWB·October 21, 2011