Summary Company Announcement Date: August 31, 2026 FDA Publish Date: August 31, 2026 Product Type: Food & Beverages Ingredients Reason for Announcement: Recall Reason Description Contains garlic essential oil not approved for culinary use Company Name: LMSI LLC Brand Name: Brand Name(s) Product Description: Product Description Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml,…
Ana Salazar Modela Tu Cuerpo Inc. Issues Nationwide Voluntary Recall of Lipofit Extreme Fat Burner 2.0 Due to Presence of Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)
Summary Company Announcement Date: August 27, 2026 FDA Publish Date: August 31, 2026 Product Type: Dietary SupplementsDrugs Reason for Announcement: Recall Reason Description Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP) Company Name: Ana Salazar Modela Tu Cuerpo Inc. Brand Name: Brand Name(s) Product Description: Product Description Lipofit Extreme 2.0 Fat Burner Dietary Supplement Company Announcement FOR IMMEDIATE…
Crystal Temptations Issues Allergy Alert on Undeclared Milk in Chocolatey Eyeballs
Summary Company Announcement Date: August 31, 2026 FDA Publish Date: August 31, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Crystal Temptations Brand Name: Brand Name(s) Little Temptations Product Description: Product Description Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz. Company…
Early Alert: Esophageal pH Monitoring Capsule Delivery Device Issue from Medtronic and Given Imaging
CDRH is issuing this Early Alert to notify the public of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available. The FDA is aware that Medtronic and their subsidiary Given Imaging, Inc. have issued a letter to affected customers recommending…
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter
Summary Company Announcement Date: August 27, 2026 FDA Publish Date: August 28, 2026 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of particulate matter identified as iron oxide Company Name: B. Braun Medical Inc. Brand Name: Brand Name(s) Product Description: Product Description 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL…
Northwest Naturals Voluntarily Recalls Two Raw Pet Food Products Because of Possible Salmonella & Listeria Monocytogenes Health Risk
Summary Company Announcement Date: August 28, 2026 FDA Publish Date: August 28, 2026 Product Type: Animal & VeterinaryFood & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential contamination with Salmonella and/or Listeria monocytogenes Company Name: Northwest Naturals Brand Name: Brand Name(s) Northwest Naturals Product Description: Product Description Chicken Recipe Company Announcement Northwest Naturals…
Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk
Summary Company Announcement Date: August 28, 2026 FDA Publish Date: August 29, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella. Company Name: Everything Sprouts, LLC Brand Name: Brand Name(s) Everything Sprouts Product Description: Product Description Robust Radish…
Panorama Produce Recalls Mangoes Due to Possible Salmonella Contamination
Summary Company Announcement Date: August 28, 2026 FDA Publish Date: August 29, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential contamination with Salmonella Company Name: Panorama Produce Brand Name: Brand Name(s) Product Description: Product Description Company Announcement MAMARONECK, NY, AUG. 28, 2026 – Panorama Produce is recalling 302…
Early Alert: Angiographic Catheter Issue from Boston Scientific
CDRH is issuing this Early Alert to notify the public of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available. Affected Product The FDA is aware that Boston Scientific has issued a letter to affected customers recommending all Imager II…
Early Alert: IV Start Kit Issue from Avid Medical
CDRH is issuing this Early Alert to notify the public of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available. Affected Product The FDA is aware that Avid Medical has issued a letter to affected customers recommending certain convenience kits affected…