Summary Company Announcement Date: June 24, 2024 FDA Publish Date: June 24, 2024 Product Type: Food & Beverages Ice Cream/Frozen Dairy Foodborne Illness Reason for Announcement: Recall Reason Description Listeria monocytogenes Company Name: Totally Cool, Inc. Brand Name: Brand Name(s) Multiple brand names Product Description: Product Description Ice Cream Products Company Announcement Totally Cool, Inc….
DSD Merchandisers, LLC Announces Voluntary Recall of Deluxe Roasted & Salted Mixed Nuts Due to Undeclared Peanut
Summary Company Announcement Date: June 24, 2024 FDA Publish Date: June 24, 2024 Product Type: Food & Beverages Nuts & Nut Products Allergens Reason for Announcement: Recall Reason Description Undeclared Peanut Company Name: DSD Merchandisers, LLC Brand Name: Brand Name(s) DSD Merchandisers, Inc. Product Description: Product Description Deluxe Roasted & Salted Mixed Nuts Company Announcement…
Vitakraft Sun Seed Recall of Sun Seed Vita Prima Hedgehog Food Due to Possible Salmonella Health Risk
Summary Company Announcement Date: June 21, 2024 FDA Publish Date: June 22, 2024 Product Type: Animal & VeterinaryFood & Beverages Pet Food Reason for Announcement: Recall Reason Description Due to potential Salmonella contamination Company Name: Vitakraft Sun Seed Inc. Brand Name: Brand Name(s) Sunseed Vita Prima Product Description: Product Description Hedgehog Food Company Announcement Vitakraft…
Snapchill LLC Recalls Canned Coffee Products Due to Potential Clostridium botulinum
Summary Company Announcement Date: June 17, 2024 FDA Publish Date: June 20, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Clostridium botulinum Company Name: Snapchill LLC Brand Name: Brand Name(s) Product Description: Product Description Coffee Products Company Announcement 06/17/2024, Snapchill LLC (Snapchill) of Green…
Infla-650 contains hidden drug ingredients
[6-20-2024] The Food and Drug Administration is advising consumers not to purchase or use Infla-650, a product promoted and sold for pain on various websites, including www.nutraherbusa.com, and possibly in some retail stores. FDA laboratory analysis confirmed that Infla-650 contains acetaminophen, diclofenac and phenylbutazone. Acetaminophen is a medicine used to reduce pain and fever that is…
Hudson Harvest Issues Voluntary Recall of Tomato Basil Sauce Due to Potential Under-Processing
Summary Company Announcement Date: June 18, 2024 FDA Publish Date: June 19, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potentially under processed, which could lead to the potential for spoilage organisms or pathogens Company Name: Hudson Harvest Brand Name: Brand Name(s) Hudson Harvest Product Description: Product Description Tomato…
Food
PDF Version (522 KB) Español The scope of FDA’s regulatory authority is very broad. FDA’s responsibilities are closely related to those of several other government agencies. Often frustrating and confusing for consumers is determining the appropriate regulatory agency to contact. The following is a list of traditionally-recognized product categories that fall under FDA’s regulatory jurisdiction;…
FDA D.I.S.C.O. Burst Edition: FDA approval of Ojemda (tovorafenib) for relapsed or refractory pediatric low-grade glioma harboring a BRAF fusion or rearrangement, or BRAF V600 mutation
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 April 23, 2024, the FDA granted accelerated approval to…
Endotracheal Tube Recall: Medline Industries, LP Removes Medline Sub-G Endotracheal Tube with Subglottic Suctioning due to Detachment or Tearing of the Inflation Tube from the Main Tube
This recall involves removing 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 Names: Medline Sub-G Endotracheal Tube with Subglottic Suctioning Unique Device Identifier (UDI)/Model: This recall includes…
Getinge Recalls Vaporizer Sevoflurane Maquet Filling for Risk of Patient and Health Care Professional Exposure to Toxic Chemical Hydrogen Fluoride
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: Vaporizer Sevoflurane Maquet Filling Product Code: 6682282 Distributed Serial Numbers: 17003 – 23454 Devices Recalled in the U.S.: 120 Dates Distributed: February 2, 2022 to…