16 results
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13ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Completed
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MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device
FDA Enforcement
Class II
·Completed·Medacta Usa Inc·April 26, 2023
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
FDA Enforcement
Class II
·Completed·Medacta Usa Inc·April 26, 2023
MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device
FDA Enforcement
Class II
·Completed·Medacta Usa Inc·April 26, 2023
MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device
FDA Enforcement
Class II
·Completed·Medacta Usa Inc·April 26, 2023
MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
FDA Enforcement
Class II
·Completed·Medacta Usa Inc·April 26, 2023
MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
FDA Enforcement
Class II
·Completed·Medacta Usa Inc·April 26, 2023
Laser Evlt Pack and Laser One Leg Evlt - contains Devon Light Glove Used during surgery
FDA Enforcement
Class II
·Completed·Stradis Healthcare, LLC.·July 15, 2015
MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device
FDA Recall
Completed
·Medacta Usa Inc·Product code OVD·March 8, 2023
MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device
FDA Recall
Completed
·Medacta Usa Inc·Product code OVD·March 8, 2023
MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device
FDA Recall
Completed
·Medacta Usa Inc·Product code OVD·March 8, 2023
MectaLIF ANTERIOR - Lag Plate Flush H10, REF 03.30.300, interbody fusion device
FDA Recall
Completed
·Medacta Usa Inc·Product code OVD·March 8, 2023
MectaLIF ANTERIOR - Lag Plate Flush H12, REF 03.30.301, interbody fusion device
FDA Recall
Completed
·Medacta Usa Inc·Product code OVD·March 8, 2023
MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
FDA Recall
Completed
·Medacta Usa Inc·Product code OVD·March 8, 2023
Laser Evlt Pack and Laser One Leg Evlt - contains Devon Light Glove Used during surgery
FDA Recall
Completed
·Stradis Healthcare, LLC.·Product code LRO·April 20, 2015
Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210
FDA Recall
Completed
·Philips Ultrasound, Inc.·Product code IYN·October 9, 2023
Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201), EPIQ 7W (Model # 795202), EPIQ 5G (model # 795204), EPIQ 5W (model # 795206), EPIQ CVx (Model # 795231), EPIQ Elite (model # 795234)
FDA Recall
Completed
·Philips Ultrasound, Inc.·Product code IYN·October 9, 2023