15 results
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12ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Completed
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Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
FDA Recall
Completed
·Cardinal Health·Product code FMI·April 30, 2019
Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
FDA Recall
Completed
·Cardinal Health·Product code FMI·April 30, 2019
Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
FDA Recall
Completed
·Cardinal Health·Product code FMI·April 30, 2019
Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
FDA Recall
Completed
·Cardinal Health·Product code FMI·April 30, 2019
Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
FDA Recall
Completed
·Cardinal Health·Product code FMI·April 30, 2019
Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
FDA Enforcement
Class II
·Completed·Cardinal Health 200, LLC·July 31, 2019
Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
FDA Enforcement
Class II
·Completed·Cardinal Health 200, LLC·July 31, 2019
Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498
FDA Enforcement
Class II
·Completed·Cardinal Health 200, LLC·July 31, 2019
Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522
FDA Enforcement
Class II
·Completed·Cardinal Health 200, LLC·July 31, 2019
Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
FDA Enforcement
Class II
·Completed·Cardinal Health 200, LLC·July 31, 2019
iLab Polaris Multi-Modality Guidance System; iLab Ultrasound Imaging System
FDA Recall
Completed
·Boston Scientific Corporation·Product code DQK·September 18, 2019
Xper Flex Cardio Physiomonitoring System, Software version 1.6.0.0388
FDA Recall
Completed
·Invivo Corporation·Product code DQK·September 24, 2018
CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is an electrophysiology measurement system used to acquire, filter, digitize, amplify, display, and record signals obtained during electrophysiological studies and related procedures. The system allows the user to monitor, display and record the signals. The system incorporates a stimulator intended to be used for diagnostic cardiac stimulation during electrophysiological testing of the heart.
FDA Recall
Completed
·CardioTek BV Amerikalaan 70 Maastricht-Airport Netherlands·Product code DQK·April 13, 2017
CardioTek EP-TRACER Software V2.x.
FDA Recall
Completed
·CardioTek BV Amerikalaan 70 Maastricht-Airport Netherlands·Product code DQK·April 25, 2022
MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c) 3101010-009, d) 3101010-008
FDA Recall
Completed
·GE Healthcare, LLC·Product code DQK·March 16, 2022