RSS: Drug safety and effectiveness monitoring
Last Updated August 6, 2020
Medtronic Announces Voluntary Recall of Unused Valiant Navion™ Thoracic Stent Graft System
Source: MedWatch Safety Alerts RSS Feed - Posted: February 23, 20212021 Medical Device Recalls
List of Medical Device recalls in 2021.…
Source: MedWatch Safety Alerts RSS Feed - Posted: February 22, 2021Pulse Oximeter Accuracy and Limitations: FDA Safety Communication
The FDA is informing patients and health care providers that pulse oximeters have limitations and a…
Source: MedWatch Safety Alerts RSS Feed - Posted: February 19, 2021Adamssecret.co Issues Voluntary Nationwide Recall of Adam’s Secret Extra Strength 1500 and 3000 Capsules Due to Presence of Undeclared Sildenafil and/or Tadalafil
Adamssecret.co is voluntarily recalling all lots within expiry of Adam’s Secret Extra Strength 1500…
Source: MedWatch Safety Alerts RSS Feed - Posted: February 16, 2021Boston Scientific Recalls EMBLEM S-ICD Subcutaneous Electrode (Model 3501) Due to Risk of Fractures
EMBLEM S-ICD Subcutaneous Electrode (Model 3501) is part of the Boston Scientific S-ICD System that…
Source: MedWatch Safety Alerts RSS Feed - Posted: February 10, 2021Using Ventilator Splitters During the COVID-19 Pandemic - Letter to Health Care Providers
Source: MedWatch Safety Alerts RSS Feed - Posted: February 9, 2021Xeljanz, Xeljanz XR (tofacitinib): Drug Safety Communication - Initial Safety Trial Results Find Increased Risk of Serious Heart-related Problems and Cancer with Arthritis and Ulcerative Colitis Medicine
Source: MedWatch Safety Alerts RSS Feed - Posted: February 4, 2021Apotex Corp. Issues Voluntary Nationwide Recall of Enoxaparin Sodium Injection, USP Due to Mislabeling of Syringe Barrel Measurement Markings
Source: MedWatch Safety Alerts RSS Feed - Posted: February 3, 2021Penumbra’s Urgent Voluntary Recall of JET 7 Catheters with Xtra Flex Technology Due to Increased Risk of Mortality and Serious Injury – Urgent Letter to Health Care Providers
Source: MedWatch Safety Alerts RSS Feed - Posted: January 29, 2021Safety Recall for Deluxe Heat Therapy Massager
Wahl Clipper Corporation is voluntarily recalling all Deluxe Heat Therapy Massagers, Model 4212.…
Source: MedWatch Safety Alerts RSS Feed - Posted: January 28, 2021Meitheal Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Cisatracurium Besylate Injection, USP 10mg per 5mL Due to Mislabeling
Source: MedWatch Safety Alerts RSS Feed - Posted: January 27, 2021Nostrum Laboratories, Inc. Expands Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 750 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit
Source: MedWatch Safety Alerts RSS Feed - Posted: January 25, 2021Boston Scientific Announces LOTUS Edge™ Aortic Valve System Voluntary Recall and Product Discontinuation
Boston Scientific Corporation (NYSE: BSX) has announced it has initiated a global, voluntary recall…
Source: MedWatch Safety Alerts RSS Feed - Posted: January 11, 2021