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: Brand Name(s) Product Description: Product Description Frozen fruits and vegetables Company Announcement Collectively (“Chetak”) is expanding its voluntary recall, initiated July…
Middlefield Original Cheese Co-Op Recalls Organic Gouda, Colored Cheddar, Mozzarella/Provolone, Pepper Jack, Swiss, Dilly Pickle Cheese and Monterey Jack Due to Possible Listeria Monocytogenes Contamination
Summary Company Announcement Date: September 05, 2025 FDA Publish Date: September 08, 2025 Product Type: Food & Beverages Cheese/Cheese Product Foodborne Illness Reason for Announcement: Recall Reason Description Potential contamination with-Listeria monocytogenes Company Name: Middlefield Original Cheese Co-op Brand Name: Brand Name(s) Middlefield Original Cheese Co-op, Sunrise Creamery Product Description: Product Description Company Announcement Middlefield,…
Endico Potatoes Inc. Recalls 2.5lb Bags of Frozen “Peas And Carrots” and “Mixed Vegetables” Because of Possible Health Risk
Summary Company Announcement Date: September 03, 2025 FDA Publish Date: September 04, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential contamination with Listeria monocytogenes Company Name: Endico Potatoes Inc. Brand Name: Brand Name(s) Product Description: Product Description Frozen Peas and Carrots, Mixed Vegetables Company Announcement ENDICO POTATOES of…
DermaRite Industries Expands Voluntary Nationwide Recall Due to Potential Burkholderia cepacia Contamination
Summary Company Announcement Date: August 27, 2025 FDA Publish Date: August 28, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Device & Drug Safety – Potential Burkholderia cepacian contamination Company Name: DermaRite Industries Brand Name: Brand Name(s) Product Description: Product Description Hand Sanitizers, Cleansers, Skin Protectants, Deodorant Company Announcement DermaRite Industries, LLC is…
Ventilator Correction: Hamilton Medical AG Corrects HAMILTON-C6 Due to Risk of Ventilation Interruption from Defective Circuit Board
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 Names: HAMILTON-C6 ventilator Unique Device Identifier (UDI)/Model: UDI: 76300028PN160021ZW Model: 160021 Lot/Serial Numbers: 13636–13950…
Properly Store Nicotine Pouches to Prevent Accidental Exposure to Children and Pets
Image Nicotine pouches can be dangerous to children if they use, touch, chew on, or eat them. These small fiber pouches, which contain nicotine that is chemically synthesized or derived from the tobacco leaf, can cause nicotine poisoning in children. It’s important to keep these products away from kids and to be prepared in case…
Ice Cream Factory Issues Allergy Alert on Undeclared Almond in Vanilla G.Nutt Ice Cream
Summary Company Announcement Date: August 29, 2025 FDA Publish Date: September 02, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared almond allergen Company Name: Ice Cream Factory Brand Name: Brand Name(s) Product Description: Product Description Vanilla G.Nutt Ice Cream Company Announcement Ice Cream Factory of Mount Vernon, NY is…
Applicator Recall: Integra LifeSciences Removes Extended Tip Applicator Due to Potential Sterility and Endotoxin Concerns
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 Catalog Number Product Name (Description) UDI-DI Lots Affected 205108 Extended Tip Applicator, 8CM, Box of…
Mobile Power Unit AC Power Cord Recall: Abbott Medical Removes AC Power Cord Associated with HeartMate Mobile Power Unit (MPU) Due to Potential Risk of the Cord Not Locking into Place
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: AC Power Cord (model: 107760) for the HeartMate Mobile Power Unit (model: 107754)…
Breathing Circuit Set Recall: Hamilton Medical, Inc. Removes Coaxial Breathing Circuit Set Due to Possible Inner Blue Tube Cracks That May Impact Ventilation
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 Part number Lot numbers Breathing circuit set, coaxial 260128 199675 Breathing circuit set,…