21 results
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15ms
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Sources: EU EUDAMED, US FDA
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Status: Terminated
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Monitor portion of the LifeVest device - specifically the Defibrillator printed circuit assembly (PCA) within the monitor. The LifeVest is indicated for adult patients who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator.
FDA Recall
Terminated
·Zoll Lifecor Corporation·Product code MVK·October 21, 2008
Model 4000 Monitor component of the LifeVest Wearable Defibrillator
FDA Recall
Terminated
·Zoll Lifecor Corporation·Product code MVK·September 24, 2010
Electrode Belt, component of the LifeVest Wearable Defibrillator, Product number 10A0889-A01. Specifically the 3 Therapy Electrode Pads attached to the Electrode Belt.
FDA Recall
Terminated
·Zoll Lifecor Corporation·Product code MVK·April 27, 2007
LifeVest Wearable Defibrillator Model 4000, Product Number 10A0988-A01. The LifeVest system is indicated for patients 18 years of age and older who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator.
FDA Recall
Terminated
·Zoll Manufacturing Corp.·Product code MVK·September 12, 2017
Battery Pack portion of the LifeVest device. The LifeVest is a wearable cardioverter defibrillator worn by a patient at risk for sudden cardiac arrest (SCA).
FDA Recall
Terminated
·Zoll Lifecor Corporation·Product code MVK·September 14, 2007
SYS IVK, Bio mCT-S(40) 3R->4R, Model Number 10250743
FDA Recall
Terminated
·Siemens Medical Solutions USA Inc.·Product code KPS·July 14, 2015
SYS IVK, Bio mCT-S(40) 3R->4R, Model Number 10250743
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA Inc.·August 12, 2015
SYS IVK, Bio mCT-S(40) 3R->4R Upgrade, MATERIAL NUMBER 10250743 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA Inc.·June 29, 2016
SYS IVK, Bio mCT-X 3R->4R Upgrade, MATERIAL NUMBER 10250745 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA Inc.·June 29, 2016
SYS IVK, Bio mCT-S(40) 3R->4R Upgrade, MATERIAL NUMBER 10250743 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
FDA Recall
Terminated
·Siemens Medical Solutions USA Inc.·Product code KPS·April 22, 2016
SYS IVK, Bio mCT-X 3R->4R Upgrade, MATERIAL NUMBER 10250745 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
FDA Recall
Terminated
·Siemens Medical Solutions USA Inc.·Product code KPS·April 22, 2016
ACUSON X700 Ultrasound System with software version 1.0.04. Model numbers: 10658844 ACUSON X700 Ultrasound System 10658846 - ACUSON X700 Ultrasound System (Russia) 10658845 - ACUSON X700 Ultrasound System (Korea) Radiology: The Siemens ACUSON X700 ultrasound imaging system is intended for the following applications: Cardiac (Adult, Pediatric), Transesphageal (Cardiac), Intracardiac, Cerebrovascular, Peripheral Vessel, Abdominal, Renal, Fetal, Abdominal, Intra-operative, Pediatric, Small Organ, Neonatal Cepahalic, Adult Cephalic, Orthopedics, Musculo-skeletal Conventional, Musculo-skeletal Superficial, Pelvic, Obstetrical, Gynecological and Urological applications. The system also provides for the measurement of anatomical structures and for analysis packages that provide information that is used for clinical diagnosis purposes.
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA, Inc.·May 4, 2016
2 pc Full Overlap Vest & Kilt, Single Item, Product Number FVK, Part Numbers REFVK*F, REFVK*M, REFVKB, REFVKD, REFVKE, REFVKF, SEFVK*F, SEFVK*M, SEFVKE, SEFVKXLM Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation reaching the user.
FDA Enforcement
Class II
·Terminated·Burlington Medical, LLC·August 7, 2019
2 pc Full Overlap Vest & Kilt, Single Item, Product Number FVK, Part Numbers REFVK*F, REFVK*M, REFVKB, REFVKD, REFVKE, REFVKF, SEFVK*F, SEFVK*M, SEFVKE, SEFVKXLM Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation reaching the user.
FDA Recall
Terminated
·Burlington Medical, LLC·Product code EAJ·June 7, 2019
Accuprobe Group B Streptococcus Culture Identification Test, Catalog Number 2820B, Batch Number 531379, Gen-Probe, Incorporated, San Diego, CA. 92121
FDA Recall
Terminated
·Gen-Probe Inc·Product code MDK·May 2, 2007
Gen-Probe AccuProbe Group B Streptococcus Culture Identification Test Kit, 2820.
FDA Recall
Terminated
·Gen-Probe Inc·Product code MDK·December 30, 2008
AcrySof ReSTOR Intraocular Lens
FDA Recall
Terminated
·Alcon Laboratories, Inc·Product code MFK·December 14, 2006
AcrySof ReSTOR Intraocular Lens
FDA Recall
Terminated
·Alcon Laboratories, Inc·Product code MFK·December 14, 2006
AcrySof Intraocular Lens
FDA Recall
Terminated
·Alcon Laboratories, Inc·Product code MFK·December 14, 2006
Sorin Platinium CRT-D 1711 DF-1, Sterile EO. Implantable Cardiac Defibrillator and Resynchronization Therapy Defibrillator
FDA Recall
Terminated
·Sorin CRM SAS Cvk 4, avenue Reaumur Clamart Cedex France·Product code NIK·July 9, 2018