FDA Issues Class I Recall for Q’Apel Medical Aspiration System: Critical Compliance Lessons for Device Manufacturers
FDA upgrades Q'Apel Medical's aspiration system recall to Class I status, affecting…
Medtronic Pipeline Vantage 027 Urgent Recall: Critical Compliance Lessons for Medical Device Manufacturers
Medtronic's urgent Pipeline Vantage 027 recall offers critical compliance lessons for medical…
FDA Updates Medline Fluid Delivery Set Alert: Key Lessons for Medical Device Manufacturers
FDA updates Medline fluid delivery set alert as part of Communications Pilot…
New Congressional Bill Could Transform Medical Device Recall Communications for Manufacturers
New bipartisan legislation could require manufacturers to use electronic recall formats and…
FDA Expands Medical Device Recall Alert Program: What Manufacturers Need to Know
FDA expands its medical device recall alert program to all devices after…
FDA Early Alert: Calyxo Aspiration System Issue Highlights New Recall Communication Strategy
FDA issues early alert for Calyxo aspiration system as part of new…
