75 results
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14ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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Bard Nasogastric Sump Tube with ENFit, 12Fr., 48in Long, REF EN0042120
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code BSS·December 20, 2023
Bard Nasogastric Sump Tube and PreVent Anti-Reflux Filter and Lopez Valve with ENFit, 18Fr., 48in Long, REF EN0056180
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FEG·December 20, 2023
Bard Nasogastric Sump Tube and PreVent Anti-Reflux Filter and Lopez Valve with ENFit, 12Fr., 48in Long, REF EN0056120
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FEG·December 20, 2023
Sensica Urine Output System, Catalog Number SCCS1002
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EXS·November 15, 2023
The Access Cortisol assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of cortisol levels in human serum, plasma (heparin, EDTA) and urine using the Access Immunoassay Systems.
FDA Recall
Open, Classified
·Beckman Coulter, Inc.·Product code CGR·September 30, 2024
DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
FDA Recall
Open, Classified
·Beckman Coulter, Inc.·Product code CGR·September 19, 2025
DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clinical Analyzer
FDA Recall
Open, Classified
·Beckman Coulter Inc.·Product code CGR·August 4, 2025
Bard Single Intragastric Linton Balloon Tube, REF: 0092740
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code KNT·April 17, 2025
Bard Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code KNT·April 17, 2025
Bard Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code KNT·April 17, 2025
Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code KNT·April 17, 2025
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8" (20.3cm) Balloon X-Ray Opaque Rubber
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code KNT·April 17, 2025
BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
Catalog A899916, SureStep" Foley Tray, Lubricath", Drainage Bag, StatLock" Stabilization Device
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZC·August 5, 2021
Catalog A119216M, SureStep" Foley Tray, Lubri-Sil", Urine Meter, Temperature Sensing Dual, StatLock" Stabilization Device
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code MJC·August 5, 2021
Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZD·April 20, 2023
Catalog A902916, SureStep" Foley Tray, Lubricath", Urine Meter, StatLock" Stabilization Device
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZC·August 5, 2021