Chetak LLC Group Expands Voluntary Product Recall to Include Additional Frozen Vegetable and Fruit Products Due to Possible Health Risk
Summary Company Announcement Date: September 10, 2025 FDA Publish Date: September 10, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Salmonella Company Name: CHETAK LLC GROUP Brand Name: Product...Gina Marie Bakery of Waterbury Issues Recall of Cookies Due to Undeclared Almonds, Sesame and Food Dyes
Summary Company Announcement Date: September 10, 2025 FDA Publish Date: September 10, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared almonds, sesame, Red 40, Red 3, Blue 1, Yellow 5, Red 40, Yellow 6...XYNTHA Lead Pge
STN: BL 125264Proper Name: Antihemophilic Factor (Recombinant), Plasma/Albumin FreeTradename: XYNTHAManufacturer: Wyeth Pharmaceuticals, LLCIndication: XYNTHA is a recombinant antihemophilic factor indicated in adults and children with hemophilia A for on-demand...Blood & Blood Products
Image The Center for Biologics Evaluation and Research (CBER) regulates the collection of blood and blood components used for transfusion or for the manufacture of pharmaceuticals derived from blood and blood components, such as clotting factors, and establishes...FDA approves selumetinib for pediatric patients 1 year of age and olde
On September 10, 2025, the Food and Drug Administration approved selumetinib (KOSELUGO, AstraZeneca Pharmaceuticals LP) granules and capsules for pediatric patients 1 year of age and older with neurofibromatosis type 1 (NF1) who have symptomatic, inoperable plexiform...KVK-Tech, Inc. Issues Voluntary Nationwide Recall of One Lot of Betaxolol Tablets, USP 10 mg (Batch Number: 17853A) as a Precautionary Measure Due to a Single Foreign Tablet Found During the Line Clearance After the Batch was Packaged
Summary Company Announcement Date: September 29, 2023 FDA Publish Date: October 03, 2023 Product Type: Drugs Reason for Announcement: Recall Reason Description Potential Presence of Oxycodone HCl tablet Company Name: KVK-Tech, Inc. Brand Name: Product Description:...Spectrum Laboratory Products, Inc. Issues Voluntary Worldwide Recall of Epinephrine (L-Adrenaline) USP Bulk Active Pharmaceutical Ingredient (API) Due to Discoloration of Product
Summary Company Announcement Date: January 09, 2023 FDA Publish Date: January 09, 2023 Product Type: Drugs Reason for Announcement: Recall Reason Description Product discoloration Company Name: Spectrum Laboratory Products Inc. Brand Name: Product Description: Company...FDA Issues New Guidance to Expand Non-Opioid Options for Chronic Pain, Curb Misuse
For Immediate Release: September 10, 2025 Despite recent declines, opioids remain commonly prescribed to about 1 in 5 U.S. adults who live with chronic pain as effective alternatives are limited. As part of its broader strategy to address the opioid crisis, the U.S....Click To Verify Security & Validation
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