Patients monitored on Portrait Mobile devices may be discharged (removed) from the Portrait monitoring system during an update to the…
Read MorePatients monitored on Portrait Mobile devices may be discharged (removed) from the Portrait monitoring system during an update to the…
Read MoreRemoval of VentStar Resus Neo hoses due to the potential for cracks resulting in restricted ventilation or delayed therapy.
Read MoreAbiomed is removing Automated Impella Controllers due to purge cassette recognition failures that may lead to prolonged delayed in mechanical…
Read MoreFOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall…
Read MoreFOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3)…
Read MoreAVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.
Read MoreCertain BD ChloraPrep Applicators in Convenience Kits manufactured by Medline may not be sterile.
Read MoreCertain reprocessed catheters may contain residual particulates that could cause infection, embolism, or thrombosis
Read MoreMedline is recalling certain neonatal and infant heated wire breathing circuits due to failures involving the electrical connector.
Read MoreBoston Scientific Imager II Angiographic Catheters removed due to a manufacturing issue leading to tip detachment; could result in procedural…
Read More