16 results
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15ms
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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
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
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
Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product Usage: The assay is an aid in the diagnosis of celiac disease (gluten-sensitive enteropathy) and should be used in conjunction with other serological tests and clinical findings.
FDA Enforcement
Class II
·Completed·Bio-Rad Labs·May 6, 2020
Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product Usage: The assay is an aid in the diagnosis of celiac disease (gluten-sensitive enteropathy) and should be used in conjunction with other serological tests and clinical findings.
FDA Recall
Completed
·Bio-Rad Labs·Product code MVM·April 3, 2019