FDA Issues Class I Recall for Q’Apel Medical’s 072 Aspiration System: Critical Safety Alert for Medical Device Manufacturers
FDA escalates Q'Apel Medical's voluntary recall of 1,617 aspiration systems to Class…
FDA Early Alert: Conavi Diagnostic Intravascular Catheter Safety Issue – What Manufacturers Need to Know
FDA issues early alert for Conavi intravascular catheters as part of enhanced…
FDA Early Alert: BD PICC Catheter Defect Highlights New Recall Communication Strategy
FDA issues early alert for BD PICC catheters as part of new…
FDA Early Alert: Medtronic Esophageal pH Monitoring Capsule Safety Issue – What Manufacturers Need to Know
FDA issues early alert on Medtronic esophageal pH capsule safety issue as…
FDA Early Alert System: Abiomed Blood Pump Controller Recall Signals New Era of Medical Device Safety
FDA's new Early Alert system for Abiomed blood pump controller signals major…
FDA Early Alert: Critical Baxter Infusion Pump Software Issue Requires Immediate Manufacturer Attention
FDA issues early alert for Baxter infusion pump software defect. Critical guidance…
