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Fresenius Kabi Recalls Ivenix Infusion Pump Software 

by Devices and Pharma | 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...

Urgent Recall for Boston Scientific Obsidio Conformable Embolic 

by Devices and Pharma | Apr 17, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls

Urgent Recall Notice for Boston Scientific Obsidio Conformable Embolic Increased bowel ischemia risk with lower GI bleeding Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...
FDA – Do Not Use Non-piercing Devices to Measure Blood Glucose

FDA – Do Not Use Non-piercing Devices to Measure Blood Glucose

by Devices and Pharma | Apr 17, 2024 | Consumer Safety, FDA Safety Communication, Med-Devices

FDA Cautions Against Using Uncleared Devices to Measure Blood Glucose Risks associated with using non-piercing devices Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...

Medos International Recalls CEREBASE DA Guide Sheath 

by Devices and Pharma | Apr 17, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, Med-Devices, Product Recalls, Product Safety

Medos International Recalls CEREBASE DA Guide Sheath Due to cracking of its distal catheter shaft Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Urgent Class I...

Asensus Surgical Inc Issues Recall for Senhance Surgical System 

by Devices and Pharma | Apr 16, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, Product Recalls

Asensus Surgical Recalls Senhance Surgical System Malfunctions with Robotic Surgical Device Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Class I Recall Notice  ...

Datex-Ohmeda Issues Field Correction for EVair Air Compressors 

by Devices and Pharma | Apr 15, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, Product Safety

Datex-Ohmeda Issues Field Correction for EVair Air Compressors Formaldehyde emissions when used with certain ventilators Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...
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