Summary Company Announcement Date: July 24, 2024 FDA Publish Date: July 24, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Kenny’s Farmhouse Cheese Brand Name: Brand Name(s) Kenny’s Farmhouse Cheese Product Description: Product Description St. Jerome cheese Company Announcement Kenny’s Farmhouse Cheese of…
JFE Franchising, Inc. Recalls A Limited Number of Products Because Of Possible Health Risk
Summary Company Announcement Date: July 25, 2024 FDA Publish Date: July 26, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: JFE Franchising, Inc. Brand Name: Brand Name(s) Product Description: Product Description Variety of vegetables and pepper mixes Company Announcement Houston, TX…
ALB-USA Enterprises Recalls ALB Flavor Ground Cinnamon Because of Possible Health Risk
Summary Company Announcement Date: July 26, 2024 FDA Publish Date: July 26, 2024 Product Type: Food & Beverages Contaminants Reason for Announcement: Recall Reason Description Potential Metal Contaminant – Lead Company Name: ALB-USA ENTERPRISES Brand Name: Brand Name(s) ALB Flavor Product Description: Product Description Ground Cinnamon Powder Company Announcement ALB-USA Enterprises, Inc. of Bronx, NY…
Supreme Service Solutions LLC Voluntarily Recalls Supreme Vegetable Products Because of Possible Health Risk
Summary Company Announcement Date: July 26, 2024 FDA Publish Date: July 26, 2024 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Supreme Service Solutions LLC Brand Name: Brand Name(s) Supreme Produce Product Description: Product Description Vegetable products Company Announcement SummaryCompany Announcement…
FDA D.I.S.C.O. Burst Edition: FDA approval of Retevmo (selpercatinib) for advanced or metastatic RET fusion-positive thyroid cancer
Podcast Welcome back to the D.I.S.C.O., FDA’s Drug Information Soundcast in Clinical Oncology, Burst Edition, brought to you by FDA’s Division of Drug Information in partnership with FDA’s Oncology Center of Excellence. Today we’ll provide a quick update on a recent FDA cancer drug approval. On May 29, 2024, the FDA granted accelerated approval to…
Safely Soothing Teething Pain in Infants and Children
[embedded content] Español Teething is a normal experience for infants and children, but it can be painful. Many well-meaning parents and caregivers who want to ease a child’s pain might turn to products that could be harmful. Soothing children’s gums with prescription or nonprescription medicines containing benzocaine or lidocaine – or homeopathic tablets and other…
Ventilator Recall: Baxter Removes Life2000 Ventilator Due to Potential Failure of Battery Charging Dongle
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Product Name: Life2000 Ventilator Unique Device Identifier (UDI): 00887761978089 What to Do Make sure there…
Aurobindo Pharma USA, Inc. on Behalf of AuroHealth, Issues Voluntary Nationwide Recall of one (1) Lot of Healthy Living Over the Counter (OTC) Migraine Relief: Acetaminophen 250mg; Aspirin 250mg; Caffeine 65mg Tablets, Due to Missing Manufacturer Label
Summary Company Announcement Date: July 18, 2024 FDA Publish Date: July 24, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Device & Drug Safety – Mislabeling Company Name: Aurobindo Pharma USA, Inc. Brand Name: Brand Name(s) Healthy Living Product Description: Product Description Migraine Relief Acetaminophen 250mg, Aspirin (NSAID) 250mg & Caffeine 65mg tablets…
What Does FDA Approve? Part 2
[embedded content] Español Is It Really “FDA Approved”? Part 2. Here are 10 more facts about how the FDA works to protect public health. Fact #11: The FDA regulates dermal fillers as medical devices. Dermal fillers are gel-like substances injected under the skin to create a smoother or fuller appearance in the lips, face, or back of…
Wildly Beloved Foods is Recalling Orzo (Vegan) Dried and Campbell (Vegan) Dried Due to Potential Mold
Summary Company Announcement Date: June 24, 2024 FDA Publish Date: June 24, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with mold Company Name: Wildly Beloved Foods Brand Name: Brand Name(s) Wildly Beloved Food Product Description: Product Description Dried Orzo and Dried Campanelle Company Announcement…