by MDP Staff | Jul 24, 2025 | Alerts-Device, Class I Recalls, Med-Devices, Product Recalls
Device Recall: ZOLL AutoPulse NXT Resuscitation System Device may fail to deliver adequate CPR Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Urgent Class I Medical Device Recall ZOLL...
by MDP Staff | Jul 24, 2025 | Alerts-Device, Corrections, Industry News, Med-Devices, Safety
Updated Use Instructions for Maquet Servo Ventilator Systems Risk in Neonatal Tidal Volume Delivery Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Maquet Servo Ventilator SystemsSource: FDA...
by MDP Staff | Jul 16, 2025 | Alerts, Alerts-Device, Class I Recalls, Product Recalls, Product Safety, Safety
Cranial Drill Urgent Recall Alert Serious safety risks Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Urgent Class I Medical Device Recall Integra LifeSciences has issued an urgent recall of...
by MDP Staff | Jul 16, 2025 | Alerts, Cardiovascular, Device Warning Letters, FDA Enforcement, FDA Public Information, FDA Warning letters, Industry News, Med-Devices, QSR, Safety
FDA Cracks Down on Insightra Medical Unapproved use and serious quality violations found Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Warning Letter Cites a Number of Serious Violations In a...
by MDP Staff | Jul 16, 2025 | Alerts, Alerts-Pharma, Consumer Safety, FDA Warning letters, Industry News, Unapproved Drugs
FDA Cracks Down on Companies Illegally Marketing 7-OH Products Products that contain 7-hydroxymitragynine (7-OH) Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Unapproved drugs sold online and...
