Tubing, Pump, Cardiopulmonary Bypass
FDA product code DWE · Class 2 · 122 devices · 43 reports · 2 deaths reported · 103 devices named in recalls
- NA BT920Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA BT926Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA 9M68RMedtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 recall0 reports
- NA BB8B89R3Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS7 reports
- BIPAL 502402BCordis US Corp. · TUBING, PUMP, CARDIOPULMONARY BYPASS6 reports
- NA 9J90R4Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS4 reports
- Intersept® 6031Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS3 reports
- NA TL10D99R2Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS2 reports
- AngioVac 25188Angiodynamics, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS2 deaths2 reports
- MHHS TMC ¼ with BB & QiD Pedi BEQ-TOP 25503Datascope Corp. · Tubing, Pump, Cardiopulmonary Bypass1 report
- Intersept® XA6061Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA 6G98RMedtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA BB8V10R2Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA TL8T46R5Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA HY6T48R10Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA 8X64R4Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA BB7P39R11Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- Intersept® 3608Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA BB8B73R7Medtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- NA BB9L12RMedtronic, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- AngioVac 25199Angiodynamics, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report
- AngioVac H965252810Navilyst Medical, Inc. · TUBING, PUMP, CARDIOPULMONARY BYPASS1 report