DLPRecalls & reported problems across all models
Medtronic, Inc. · 151 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
DLP models — page 2
151 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- DLP® 69328Catheter, cannula and tubing, vascular, cardiopulmonary bypass3 reports
- DLP® 20012SCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS3 reports
- DLP® 94835CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS3 reports
- DLP® 12112CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 death3 reports
- DLP® 50010CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS3 reports
- DLP® 75324CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS3 reports
- DLP® 71424CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS3 reports
- DLP™ CB77016Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP® 69331Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP® 10218CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 death2 reports
- DLP® 10014CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 10012CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 96428CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 10051SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 reports
- DLP® 69324CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 94735CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 94745CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP® 89022CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 reports
- DLP™ 77012Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP™ 77016Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP™ 77116Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 reports
- DLP™ CB67312Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- DLP™ CB67532Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- DLP® 69316Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- DLP® 20014LCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 20009CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 12218CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 31002CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 94535CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 79003CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- DLP® 14001Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass1 report
- DLP® 50011CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 10534Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass1 report
- DLP® 80120CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 10007Adaptor, stopcock, manifold, fitting, cardiopulmonary bypass1 report
- DLP® 66114CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 69314CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 69312CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 68112CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 77108CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 87024CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 89124CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 71422CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 94975CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 88020CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 88024CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 70422CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP® 70424CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS1 report
- DLP™ 77108Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- DLP™ 77012Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
- DLP™ 77210Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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