Summary Company Announcement Date: November 12, 2025 FDA Publish Date: November 13, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Salmonella Company Name: Food To Live Brand Name: Brand Name(s) Food To Live Product Description: Product Description Organic Supergreens Powder Mix and Organic Moringa…
Update: FDA Encourages the Public to Follow Established Choking Rescue Protocols – FDA Safety Communication
Español 简体中文 (Simplified Chinese) Tagalog Update: November 13, 2025 The FDA has taken actions to address the marketing of unauthorized anti-choking devices, including issuing Warning Letters and an Import Alert. Additional information is provided below under the FDA Actions section. Date Issued: April 22, 2024 The U.S. Food and Drug Administration (FDA) encourages the public to follow…
ByHeart Broadens Voluntary Recall While Investigation Continues
Summary Company Announcement Date: November 11, 2025 FDA Publish Date: November 11, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Clostridium botulinum Company Name: ByHeart Inc. Brand Name: Brand Name(s) Product Description: Product Description Whole Nutrition Infant formula 24 oz cans and 0.6oz packets Company…
In Response to a Broader FDA Investigation, ByHeart Initiates a Voluntary Recall of Two Batches of Infant Formula
Summary Company Announcement Date: November 08, 2025 FDA Publish Date: November 08, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Clostridium botulinum Company Name: ByHeart Inc. Brand Name: Brand Name(s) Product Description: Product Description Whole Nutrition Infant formula Company Announcement [New York, NY] – ByHeart, a next-generation…
Fresenius Kabi Issues Voluntary Nationwide Recall of Three Lots of Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL Fill in a 2 mL Vial Due to Out-of-Specification Endotoxin Results in Certain Reserve Samples
Summary Company Announcement Date: November 06, 2025 FDA Publish Date: November 07, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Out-of-specification endotoxin results Company Name: Fresenius Kabi USA, LLC Brand Name: Brand Name(s) Fresenius Kabi Product Description: Product Description Famotidine Injection, USP 20 mg per 2 mL Company Announcement Nov. 6,2025 – LAKE…
Blue Oven Bakery, Inc. Issues a Voluntary Recall Due to Undeclared Milk Allergens in Their English Muffin
Summary Company Announcement Date: October 31, 2025 FDA Publish Date: November 06, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Blue Oven Bakery, Inc. Brand Name: Brand Name(s) Blue Oven Bakery, Inc. Product Description: Product Description English muffin Government Agency Partner Announcement Cincinnati, Ohio (October 31, 2025)…
Africa Imports Issues Voluntary Recall of Organic Moringa Leaf Powder Due to Potential Salmonella Contamination
Summary Company Announcement Date: November 06, 2025 FDA Publish Date: November 06, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential to be contaminated with Salmonella Company Name: Africa Imports Brand Name: Brand Name(s) Africa Imports Product Description: Product Description Organic Moringa Leaf Powder Company Announcement Africa Imports is voluntarily recalling…
African Food on Wheels Inc. Recalls Oven Dried Fish (Scomberomorus Cavalla) Because of Possible Health Risk
Summary Company Announcement Date: November 05, 2025 FDA Publish Date: November 06, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential to be contaminated with Clostridium botulinum Company Name: African Food on Wheels Inc. Brand Name: Brand Name(s) African Food on Wheels Inc. Product Description: Product Description Oven Dried Fish (Scomberomorus…
Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 20 mEq Potassium Chloride Injection Due To Overwrap Mislabeled As 10 mEq Potassium Chloride Injection
Summary Company Announcement Date: October 31, 2025 FDA Publish Date: November 03, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Potential for Potassium chloride overdose: 20 mEq Potassium Chloride Injection is Mislabeled As 10 mEq Potassium Chloride Injection Company Name: Otsuka ICU Medical LLC Brand Name: Brand Name(s) ICU Medical Product Description: Product…
Dreyer’s Grand Ice Cream, Inc. Issues Allergy Alert on Undeclared Wheat in Haagen-Dazs Chocolate Dark Chocolate Mini Bars in 6 Count Pack
Summary Company Announcement Date: November 03, 2025 FDA Publish Date: November 04, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description May contain undeclared wheat Company Name: Dreyer’s Grand Ice Cream, Inc. Brand Name: Brand Name(s) Haagen-Dazs Product Description: Product Description Ice Cream Bars Company Announcement November 3, 2025, Dreyer’s Grand Ice…