250 results
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18ms
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Sources: EU EUDAMED, US FDA
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Status: Completed
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Centricity Universal Viewer Zero Footprint Client, Model Number 2090258-001, Software Versions 6.0 SP7, SP7.0.1, SP7.0.2, SP7.0.3, SP8, SP8.0.1, SP8.0.a and SP8.0.2, SP9 and SP9.0.1 display o orientation markers can become is incorrect.
FDA Recall
Completed
·GE Healthcare, LLC·Product code LLZ·November 9, 2018
IntelliSpace PACS 4.4, Product number 837507 - Product Usage: intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians.
FDA Recall
Completed
·Philips Healthcare Informatics, Inc.·Product code LLZ·April 19, 2019
Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S
FDA Recall
Completed
·Covidien Llc·Product code GDW·November 23, 2020
Covidien TA Auto Suture Vascular Loading Unit with DST Series Technology 30 mm- V3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3L
FDA Recall
Completed
·Covidien Llc·Product code GDW·November 23, 2020
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
FDA Recall
Completed
·Acumed LLC·Product code HWC·March 9, 2022
4.0mm x 12mm Cannulated Screw, Short Thread; Part number 3005-40012
FDA Recall
Completed
·Acumed LLC·Product code HWC·March 9, 2022
Pediatric Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Suction Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Upper Extremity Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Podiatry Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Lipo/Buttocks Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
SIGNA Creator, SIGNA Explorer nuclear magnetic resonance imaging system
FDA Recall
Completed
·GE Healthcare, LLC·Product code LNH·August 26, 2021
SynCardia 50cc TAH-t, Clinical, REF 570500, Sterile EO
FDA Recall
Completed
·SynCardia Systems LLC·Product code LOZ·August 1, 2023
Vasc Custom Kit - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Plastic Pack and Plastic HNP Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Neurosurgery Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Discovery MR750w 3.0T nuclear magnetic resonance imaging system
FDA Recall
Completed
·GE Healthcare, LLC·Product code LNH·August 26, 2021
SIGNA Voyager nuclear magnetic resonance imaging system
FDA Recall
Completed
·GE Healthcare, LLC·Product code LNH·August 26, 2021
Revolution CT
FDA Recall
Completed
·GE Healthcare, LLC·Product code JAK·March 19, 2021
Lima Pack - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015