by Devices and Pharma | Mar 17, 2023 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, Med-Devices, Product Recalls, Product Safety, US-FDA
Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Software issue can cause potential harm or death On March 10, the US Food and Drug Administration (FDA) announced...
by Devices and Pharma | Feb 26, 2023 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, Industry News, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA
Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact 1200-pound Devices Could Fall on Patients On February 15, the FDA issued a statement announcing a recall of certain...
by Devices and Pharma | Feb 12, 2023 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, US-FDA
FDA Announces Recall of LivaNova LifeSPARC System Home About Consumer Medical Devices New Devices Safety Alerts Warning Letters Pharma New Drug Approvals Drug Shortages Safety Alerts Warning Letters Regulatory Services 510(k) Submissions Documentation News Enforcement...
by Devices and Pharma | Dec 31, 2022 | Alerts, Alerts-Pharma, Class I Recalls, Consumer Safety, Industry News, Pharmaceuticals, Product Recalls, Product Safety, US-FDA
Hospira Recalls Antibiotic for Presence of Glass Particles Product was distributed throughout the U.S. and Puerto Rico Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...
