by Bruce Waldon | Feb 16, 2026 | Alerts, Alerts-Supplements, Consumer Information, Consumer Safety, Dietary Supplements, DSHEA, Industry News, Legislation, MedWatch-System, Product Recalls, Product Safety, Reg_Products
Live it Up Super Greens Recalled A second invisible outbreak of moringa root powder Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation Contact Live it Up Super...
by Bruce Waldon | Dec 13, 2025 | Dietary Supplements, DSHEA, Editorial, FDA Enforcement, Industry Information, Industry News, Legislation, MedWatch-System, Product Quality
Do Not Blame FDA for Lax Oversight of Dietary Supplements MDP Policy Commentary Home Request Info QMSR Central QMSR FAQs ISO 13485 Transition Impact Integration Definitions FDA and ISO 13485 ISO 9000 Small Manufacturers A Regulatory System Designed to Fail The recent...
by Bruce Waldon | Dec 11, 2025 | Alerts, Alerts-Supplements, Consumer Information, Dietary Supplements, DSHEA, Industry Information, Industry News, Legislation, MedWatch-System, Product Quality, Quality Information, Safety
The 30-Year Consequences of DSHEA A direct cause of the supplement safety crisis Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact How a 1994 Law Created Today’s...
by Devices and Pharma | Jul 10, 2025 | Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, Products_Devices, Safety, US-FDA
AirLife/Vyaire Infant Breathing Systems Recall Potential for risk of disconnection Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Class I Recall AirLife and manufacturer Vyaire are recalling...
by Devices and Pharma | Jul 10, 2025 | Alerts-Device, Class I Recalls, FDA Safety Communication, Industry News, Med-Devices, MedWatch-System, Product Recalls, US-FDA
Avanos Recalls Ballard Closed Suction Systems Due to sterilization failure Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact May result in non-sterile devices Avanos Medical, Inc. is recalling its...
by Devices and Pharma | Jul 8, 2025 | Alerts-Device, Class I Recalls, FDA Safety Communication, Med-Devices, MedWatch-System, Product Recalls, Product Safety
FDA Alert: Abiomed Impella Blood Pump Urgent Recall Controller may fail to detect the Impella device Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Abiomed Impella blood pump controllers...
