224 results
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18ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Guidant Acrobat Vacuum Stabilizer, Model Number OM-9000.
FDA Recall
Terminated
·Guidant Cardiac Surgery·Product code MWS·December 1, 2006
Octopus Evolution AS Tissue Stabilizer, Model TS2500
FDA Recall
Open, Classified
·Medtronic Perfusion Systems·Product code MWS·May 12, 2026
Titan" Stabilizer Attachment and Titan TM 360 Stabilizer Attachment
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corporation·Product code MWS·January 5, 2015
Hercules 360 Universal Stabilizing Arm, top mount, 360-degree rotation, reusable stainless steel
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corporation·Product code MWS·August 20, 2014
XPOSE 4 Access Device (XP-4000) XPOSE 3 Access Device (XP-3000) positioners. Product Usage: The OM-9100S Acrobat V Vacuum Off-Pump System is intended for use during performance of cardiac surgical procedures through a sternotomy incision. The stabilizer isolates and provides local immobilization of a vessel on the beating heart.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MWS·November 16, 2011
Guidant Acrobat Vacuum Stabilizer, Model number-OM-9100
FDA Recall
Terminated
·Guidant Cardiac Surgery·Product code MWS·December 1, 2006
Consist of a distal connection mechanism (either standard Terumo Ball Quick Connect or Terumo Shaft Quick Connect), an articulating arm with links, a handle for providing cable tension, and a mechanism to mount the device to a sternal retractor.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corporation·Product code MWS·March 2, 2021
Octopus 4 Tissue Stabilizer, Model 29400
FDA Recall
Open, Classified
·Medtronic Perfusion Systems·Product code MWS·May 12, 2026
Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump System OM-9000S Axius Xpose 3 Access Device XP-3000 XPOSE 4 Access Device XP-4000 Acrobat V Vacuum Off-Pump System Each Acrobat V Vacuum Off-Pump system is intended for use during performance of cardiac surgical procedures through a sternotomy incision approach.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MWS·August 13, 2014
Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1
FDA Recall
Open, Classified
·Medtronic Perfusion Systems·Product code MWS·January 13, 2026
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z
FDA Recall
Open, Classified
·Maquet Cardiovascular, LLC·Product code MWS·October 16, 2024
ACROBAT Stabilizers- ACROBAT V Vacuum Off-Pump System (OM-91 OOS), ACROBAT SUV Vacuum Off-Pump System (OM-9000S), ACROBAT Mechanical Off-Pump System (OM-6000S) Product Usage: The OM-9100S Acrobat V Vacuum Off-Pump System is intended for use during performance of cardiac surgical procedures through a sternotomy incision. The stabilizer isolates and provides local immobilization of a vessel on the beating heart.
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code MWS·November 16, 2011
Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z
FDA Recall
Open, Classified
·Maquet Cardiovascular, LLC·Product code MWS·October 16, 2024
Acrobat-i Vacuum Positioner System, Model Number XP-5000Z
FDA Recall
Open, Classified
·Maquet Cardiovascular, LLC·Product code MWS·October 31, 2023
Octopus Evolution Tissue Stabilizer, Model TS2000
FDA Recall
Open, Classified
·Medtronic Perfusion Systems·Product code MWS·May 12, 2026
Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a sternotomy incision approach. Product Code: OM-10000Z
FDA Recall
Open, Classified
·Maquet Cardiovascular, LLC·Product code MWS·September 13, 2023
Acrobat-i Positioner. Model Number C-XP-5000Z
FDA Recall
Open, Classified
·Maquet Cardiovascular, LLC·Product code MWS·October 16, 2024
Disposable Surgical Level 3 Gown, Size/Product Code: Large/GWS-03-L-B, XLarge/GWS-03-XL-B, XXLarge/GWS-03-XXL-B
FDA Recall
Open, Classified
·Texas Medical Technology Inc.·Product code FYA·September 1, 2022
Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to facilitate functional gait training of subjects with gait and/or balance impairment by providing dynamic partial vertical unloading during walking on a treadmill. The device will be used as an assistive device for gait deficiency rehabilitation and research purposes.
FDA Recall
Open, Classified
·MOTEK MEDICAL B.V. Hogehilweg 18 18 Unit C Amsterdam Netherlands·Product code BXB·July 29, 2019
Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS
FDA Recall
Open, Classified
·ARROW INTERNATIONAL Inc.·Product code DSP·April 29, 2024