News

Abbott Proclaim Implantable Pulse Generators Battery ERI

Recall of Abbott Proclaim Implantable Pulse Generators – Battery Elective Replacement Indicator (ERI) According to the U.S. Food and Drug Administration, this …

Medtronic PB500 Series Ventilators Length of Cumulative Use

Urgent Field Safety Notice: Medtronic Puritan Bennett 500 Series Ventilators – Length of Cumulative Use According to the manufacturer, this Urgent Field …

GE Healthcare CARESCAPE B650 CASESCAPE B850 CASESCAPE Canvas 1000 CARESCAPE Canvas Smart Display CPU Battery

Recall of GE Healthcare CARESCAPE B650, B850, Canvas 1000 and Canvas Smart Display Patient Monitors – CPU Timekeeper Battery According to the …

Alcon Research ClearCut Knives Recall-Dull Blades

Recall of Alcon Research ClearCut Knives – Dull Blades According to the U.S. Food and Drug Administration, this recall involved a device …

Agilent Tech Dako CoverStainer Plexiglass Front Door

Recall of Agilent Technologies Dako CoverStainer – Front Plexiglass Cover According to the U.S. Food and Drug Administration, this recall involved a …

Philips Respironics OmniLab Advanced Plus Recall

Recall of Philips Respironics OmniLab Advanced Plus Ventilators – Inoperative Alarm According to the U.S. Food and Drug Administration, this recall involved …

Equiptrack TruAsset CMMS Customers

Equiptrack provides Recall data to TruAsset CMMS Customers Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper …

Stryker HeartSine Samaritan PAD AEDs

Recall of Stryker HeartSine Samaritan PAD Model AEDs According to the U.S. Food and Drug Administration, this recall involved a device in …

Baxter Healthcare Spectrum IQ IV Pump - Front panel mount cracks

Recall of Baxter Healthcare Spectrum IQ IV Pumps – Front panel mount cracks According to the U.S. Food and Drug Administration, this …

Siemens ACUSON Ultrasound Systems-Cardiac DICOM SR

Recall of Siemens ACUSON Ultrasound Systems-Cardiac DICOM SR According to the U.S. Food and Drug Administration, this recall involved a device in …

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