Medtronic DLP Left Heart Vent Catheter Recall: Critical Lessons for Cardiovascular Device Manufacturers
Medtronic's DLP Left Heart Vent Catheter recall highlights critical compliance lessons for…
Olympus Polyloop Recall: Critical Lessons for Medical Device Post-Market Surveillance
Olympus's voluntary Polyloop corrective action offers critical lessons for medical device manufacturers…
GAO Report Exposes Critical FDA Staffing Gaps Affecting Medical Device Recall Oversight
GAO audit reveals FDA staffing shortages are delaying medical device recall oversight,…
Congressional Push for Electronic Medical Device Recall Reporting: What Manufacturers Need to Know
Senators Durbin and Schakowsky propose electronic recall reporting for medical devices. Learn…
GAO Report Exposes Critical FDA Staffing Gaps in Medical Device Recall Oversight
GAO investigation reveals FDA staffing shortages are delaying medical device recall oversight,…
Medical Device Recall Improvement Act Reintroduced: What Manufacturers Need to Know
New legislation could transform medical device recall communications with mandatory electronic notifications…
