Summary Company Announcement Date: October 17, 2025 FDA Publish Date: October 17, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Metal Contaminant – Lead Company Name: Haitai, Inc Brand Name: Brand Name(s) Product Description: Product Description Ground cinnamon Company Announcement Haitai, Inc of Cerritos, CA (Oct., 15, 2025) is recalling…
Nat’s Nuts Issues Allergy Alert on Potential Undeclared Cashews in Nat’s Nuts Brand Cinnamon Whiskey Pecans
Summary Company Announcement Date: October 17, 2025 FDA Publish Date: October 17, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared cashews Company Name: Nat’s Nuts Brand Name: Brand Name(s) Nat’s Nuts Product Description: Product Description Cinnamon Whiskey Pecans Company Announcement Nat’s Nuts of Rochester, NY is recalling 600 bags of…
Kenz Henz Recalls “Pastured Raised Eggs” Because of Possible Health Risk
Summary Company Announcement Date: October 16, 2025 FDA Publish Date: October 17, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential to be contaminated with Salmonella Company Name: Kenz Henz Brand Name: Brand Name(s) Product Description: Product Description Grade AA Large Pasture Raised Eggs Company Announcement Kenz Henz of Santa Fe,…
Jody’s Inc. Recalls Cabot Creamery Sea Salt Caramel Cheddar Popcorn Due to Undeclared Peanuts
Summary Company Announcement Date: October 17, 2025 FDA Publish Date: October 17, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Due to presence of undeclared peanuts Company Name: Jody’s Inc. Brand Name: Brand Name(s) Cabot Creamery Product Description: Product Description Sea Salt Caramel Cheddar Popcorn Company Announcement NORFOLK, VIRGINIA –…
Potential Risks with Certain Uses of Radiofrequency (RF) Microneedling – FDA Safety Communication
Date Issued: October 15, 2025 The U.S. Food and Drug Administration (FDA) is making consumers, patients, and health care providers aware that serious complications have been reported with certain uses of radiofrequency (RF) microneedling devices. These devices use an array of small electrodes, also known as microneedles, to deliver RF energy into and under the…
Ben’s Original™ Issues Voluntary Recall of Select Ben’s Original Long Grain White, Whole Grain Brown, and Long Grain & Wild Ready Rice Products Due to Possible Presence of Small Stones from Farm
Summary Company Announcement Date: October 10, 2025 FDA Publish Date: October 14, 2025 Product Type: Food & Beverages Contaminants Reason for Announcement: Recall Reason Description Potential Foreign Body Contaminant – Small Stones Company Name: Ben’s Original Brand Name: Brand Name(s) Ben’s Original Product Description: Product Description Long Grain White, Whole Grain Brown, and Long Grain…
Alert: Automated Impella Controller Correction due to Cybersecurity Issue from Abiomed
This recall involves correcting devices and does not involve removing them 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 without correction. Affected Product Product Code(s) Product Description(s) UDI-DI(s) Impacted Serial Numbers…
Raw Bistro Pet Fare Voluntarily Recalls Frozen Beef Entrée Because of Possible Salmonella Health Risk
Summary Company Announcement Date: October 10, 2025 FDA Publish Date: October 10, 2025 Product Type: Animal & VeterinaryFood & Beverages Pet Food Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Raw Bistro Pet Fare Brand Name: Brand Name(s) Raw Bistro Product Description: Product Description Frozen Beef Dog Food…
FDA Approves Labeling Changes that Include a Boxed Warning for Immune Effector Cell-associated Enterocolitis Following Treatment with Ciltacabtagene Autoleucel (CARVYKTI, Janssen Biotech, Inc.)
AUDIENCE: Patient, Health Care Professional, Pharmacy, Gastroenterology ISSUE: The FDA has received reports of immune effector cell-associated enterocolitis (IEC-EC) in patients who received treatment with CARVYKTI. Reports were received from clinical trials and postmarketing adverse event data. Patients with IEC-EC presented with severe or prolonged diarrhea, abdominal pain, and weight loss requiring total parenteral nutrition….
Sprouts Farmers Market is Recalling Smoked Mozzarella Pasta Salad Because of Possible Health Risk
Summary Company Announcement Date: October 08, 2025 FDA Publish Date: October 09, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Sprouts Farmers Market Brand Name: Brand Name(s) Product Description: Product Description Smoked Mozzarella Pasta Salad Company Announcement October 8, 2025, Sprouts…