184 results
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21ms
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Sources: EU EUDAMED, US FDA
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Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant Model/Catalog Number: OSTF-3 (Sz. 3), OSTF-4 (Sz. 4), OSTF-5 (Sz. 5) Software Version: N/A Product Description: The Osteotec Silicone Finger Implant is a one-piece, sterile, flexible silicone elastomer implant which is placed, during arthroplasty, in the proximal and distal intramedullary canals of either metacarpophalangeal (MCP) or proximal interphalangeal (PIP) joints. The implant is not fixed into the bones and becomes stabilized by the encapsulation process. The implant is available in eleven sizes to meet various anatomical variations and is supplied sterile. Component: N/A
FDA Recall
Open, Classified
·Osteotec Limited·Product code KYJ·June 18, 2025
LeadCare Blood Lead Testing System Kits Catalog Number: 70-2233
FDA Recall
Terminated
·Esa Biosciences, Inc.·Product code DOF·May 19, 2005
ESA LeadCare II Blood Test Kit, 6 test Kit containing Level 1 and Level 2 Control Vials with lot number: 0704A Catalog Number: 70-7142
FDA Recall
Terminated
·Esa Biosciences, Inc.·Product code DOF·September 20, 2007
ESA LeadCare II Blood Test Kit containing Level 1 and Level 2 Control Vials with lot number: 0704A Catalog Number: 70-6762
FDA Recall
Terminated
·Esa Biosciences, Inc.·Product code DOF·September 20, 2007
3M ESPE Rely X Veneer Cement Refill Syringes, A3 Opaque/Yellow Opaque Shade, manufactured by 3M. ESPE is a radiopaque , color stable light-cured resin cement indicated for bonding veneers fabricated of porcelainor composite.
FDA Recall
Terminated
·3M Espe Dental Products·Product code EBF·February 12, 2007
IntelePACS (Image Fusion Module) - InteleViewer
FDA Recall
Open, Classified
·INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada·Product code LLZ·February 5, 2025
IntelePACS - InteleConnect / TechPortal
FDA Recall
Open, Classified
·INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada·Product code LLZ·October 17, 2025
GE Datex-Ohmeda Advance Anesthesia Gas-Machine.
FDA Recall
Terminated
·GE Healthcare·Product code BSZ·February 5, 2009
Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray DS USA Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 This is a device used to administer to a patient continuously or intermittently a general inhalation anesthetic and to maintain a patient's ventilation.
FDA Recall
Terminated
·Mindray DS USA, Inc. d.b.a. Mindray North America·Product code BSZ·August 13, 2012
Newport Portable Package, Model #50000, Serial # 13591, 13592, 13604, 13606, 13614, 13662, 13663, 13664, 13726, 13731, 13733, 13736, 13737, 13738, 13740, 13768, 13770, 13771, 13772, 13784, 13787. Product Usage: Portable Analgesia Gas Machine.
FDA Recall
Terminated
·Accutron Inc·Product code BSZ·April 29, 2012
CM Flowmeter Pkg H, Model #36700, Serial # 13749 Product Usage: Conscious Sedation Unit Analgesia Gas Machine.
FDA Recall
Terminated
·Accutron Inc·Product code BSZ·April 29, 2012
GE Healthcare, Avance, Avance CS2, Aisys, Aespire View, and Engstrom. Intended for volume or pressure control ventilation.
FDA Recall
Terminated
·GE Healthcare, LLC·Product code BSZ·August 28, 2013
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.
FDA Recall
Terminated
·MCKESSON TECHNOLOGIES INC.·Product code BSZ·March 15, 2013
GE Datex-Ohmeda ADU Carestation Intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients.
FDA Recall
Terminated
·GE Healthcare·Product code BSZ·October 30, 2008
DCI Equipment Track Mount Light Assembly, 110v
FDA Recall
Terminated
·Dental Equipment LLC·Product code EAZ·May 1, 2007
Datex-Ohmeda S/5 Aespire Anesthesia System 7100
FDA Recall
Terminated
·Datex-Ohmeda Inc·Product code BSZ·September 27, 2005
GE, 1011-9000-000 Aisys Anesthesia Machine and Monitor
FDA Recall
Terminated
·Ge Healthcare, Llc·Product code BSZ·March 12, 2010
FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalation anesthesia on neonatal to adult patient populations.
FDA Recall
Terminated
·Maquet Cardiovascular Us Sales, Llc·Product code BSZ·April 2, 2015
GE Healthcare, Aisys, 1011-9000-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventilation. The Aisys is not suitable for use in a MRI environment.
FDA Recall
Terminated
·GE Medical Systems, LLC·Product code BSZ·December 15, 2015
GE Healthcare, Aisys CS2,1011-9050-000; Avance Amingo,1009-9002-000, & Avance CS2, 1009-9050-000. The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventilation. The Aisys is not suitable for use in a MRI environment.
FDA Recall
Terminated
·GE Medical Systems, LLC·Product code BSZ·December 15, 2015