154 results
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13ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Completed
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Gambro ClinicalKit Safety Kit 15G, Catalog Number 0141080405C. Packaged 30 kits per case. Each kit contains 2 Nipro Safetouch Safety Needles.
FDA Recall
Completed
·Gambro Renal Products·November 13, 2002
Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery
FDA Enforcement
Class II
·Completed·Stradis Healthcare, LLC.·July 15, 2015
POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 8F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; NAUTILUS DELTA Tip Confirmation System (Includes: Netbook with Pre-loaded Software, Patient Module, and ECG Cable) Product Usage: Is an implantable access device designed to provide repeated access to the vascular system.
FDA Recall
Completed
·Bard Peripheral Vascular Inc·Product code LJT·June 25, 2018
POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 8F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; NAUTILUS DELTA Tip Confirmation System (Includes: Netbook with Pre-loaded Software, Patient Module, and ECG Cable) Product Usage: Is an implantable access device designed to provide repeated access to the vascular system.
FDA Enforcement
Class II
·Completed·Bard Peripheral Vascular Inc·July 31, 2019
IceSeed" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceRod" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceSeed" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
Five IceSphere" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceRod" i-Thaw" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceRod" He-Thaw Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceRod" i-Thaw" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceFORCE" 2.1 CX Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IcePearl" 2.1 CX Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
Peak Universal Bond Self-Etch Bottle Kit, Part: 4541; Peak Universal Bond Self-Etch Intro Kit, Part: 4554; Peak SE Primer 4pk Refill, Part: 5135; Peak Universal Bond Sample SE, Part: S4554. For use in light-curing dental bonding procedures.
FDA Recall
Completed
·Ultradent Products, Inc.·Product code KLE·June 1, 2022
Five IceRod" i-Thaw" Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
Three IcePearl" 2.1 CX Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
Three IceFORCE" 2.1 CX Prostate Cryoablation Kit
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceSeed" Prostate Cryoablation Kit
FDA Enforcement
Class II
·Completed·Boston Scientific Corporation·December 30, 2020
IceRod" Prostate Cryoablation Kit
FDA Enforcement
Class II
·Completed·Boston Scientific Corporation·December 30, 2020