Fast Company Spotlights Critical Gaps in Medical Device Recall Process: What Manufacturers Need to Know
Fast Company highlights critical gaps in medical device recall processes, emphasizing the…
FDA Expands Early Alert Pilot Program: What Medical Device Manufacturers Need to Know
FDA expands Early Alert pilot program beyond initial five device categories, creating…
High-Risk Medical Device Recalls of 2024: Legal Consequences and Compliance Lessons
Major 2024 medical device recalls including BioZorb, Cartiva, and Impella have triggered…
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…
