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Important Recall Notice for BioMérieux VITEK 2 AST Kit 

by Bruce Waldon | Apr 30, 2024 | Alerts, Alerts-Device, Class I Recalls, Industry News, Med-Devices, Pharmaceuticals, Product Recalls

Recall Notice for BioMérieux VITEK 2 AST Kit An anomaly in Ceftriaxone concentrations results in misreading bacterial susceptibility Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Class I Recall Notice  ...

SonarMed Inc Recalls Airway Acoustic Sensors

by Bruce Waldon | Apr 29, 2024 | Alerts-Device, Class I Recalls, Industry News, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA

SonarMed Inc. Recalls Airway Acoustic Sensors Restriction of inner diameter may impede catheter passage Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Urgent Class I Recall Notice   SonarMed Inc. has issued...

DeRoyal Industries, Inc. Recalls Tracecarts

by Bruce Waldon | Apr 28, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Information, Med-Devices, MedWatch-System, Product Recalls, Product Safety

DeRoyal Industries, Inc. recalls Tracecarts under recall by Nurse Assist Contents include 16FR Urine Meter Foley catheter Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...

Class I Recall for Stay-Safe Catheter Extension Sets and Adapters 

by Bruce Waldon | Apr 27, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, Industry News, Med-Devices, Product Recalls, Product Safety, US-FDA

Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and Stay-Safe Adapter High risk of exposure to toxic compound NDL-PCBA Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts...

Abbott/Thoratec Recalls HeartMate II and HeartMate 3 LVAS

by Bruce Waldon | Apr 21, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA

Abbott/Thoratec Corp. Recalls HeartMate II and HeartMate 3 Biological material buildup may obstruct flow Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Recall Alert: HeartMate II and HeartMate 3 Left...

Fresenius Kabi Recalls Ivenix Infusion Pump Software 

by Bruce Waldon | Apr 17, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, Product Recalls, Product Safety

Fresenius Kabi Recalls Ivenix Infusion Pump Software Software anamolies could cause patient harm and fatalities Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact...
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