Major Eye Drop Recall Shows Manufacturing and Inspection Issues

by | Apr 18, 2026 | Alerts-Pharma, Consumer Information, Consumer Safety, Industry Information, Industry News, MedWatch-System, Product Quality, Product Recalls, Products_Drugs, Quality system, Sterilization

Home About Consumer News Food and Beverage Supplements Cosmetics Regulatory Medical Devices Pharma Biologics Combination Products In Vitro Diagnostics Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation Contact Massive eye drop recall reflects...

Kian Pee Wan Capsules Recalled for Undeclared Drug Ingredients

by | Apr 18, 2026 | Alerts-Pharma, Alerts-Supplements, Consumer Information, Dietary Supplements, FDA Safety Communication, Pharmaceuticals, Product Ingredients, Products_Drugs

FDA Recall Notification Kian Pee Wan Capsules Home About Consumer News Food and Beverage Supplements Cosmetics Regulatory Medical Devices Pharma Biologics Combination Products In Vitro Diagnostics Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation...

Blaine Labs Recalls Wound Care Gels for Microbial Contamination

by | Apr 13, 2026 | Alerts, Alerts-Pharma, Consumer Information, FDA Safety Communication, Industry Information, Industry News, Pharmaceuticals, Products_Drugs, Safety, US-FDA

FDA Recall Notification Blaine Labs wound care gels Home About Consumer News Food and Beverage Supplements Cosmetics Regulatory Medical Devices Pharma Biologics Combination Products In Vitro Diagnostics Veterinary AI Quality QMSR Central News Enforcement Alerts...

Testosterone Regulation Takes a Sharp Turn

by | Dec 18, 2025 | Alerts-Pharma, Analysis, Consumer Information, Consumer Safety, Editorial, FDA Policy, FDA Regulations, Hormones, Industry Information, Industry News, Product Safety, Products_Drugs, Regulatory_Info

Testosterone Regulation Takes a Sharp Turn Why FDA’s December panel raises red flags Home Request Info QMSR Central QMSR FAQs ISO 13485 Transition Impact Integration Definitions FDA and ISO 13485 ISO 9000 Small Manufacturers Why FDA’s December Panel Raises Red Flags...