Summary Company Announcement Date: June 20, 2025 FDA Publish Date: June 20, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description SE Grocers Company Name: Undeclared milk allergen Brand Name: Brand Name(s) SE Grocers Product Description: Product Description Dark chocolate nonpareils Company Announcement International Foodsource, LLC of Randolph NJ is recalling…
Sabores Bakery, Dba Sabores A Tu Mesa, Issues Allergy Alert on Undeclared Milk in Mousse Desserts
Summary Company Announcement Date: June 20, 2025 FDA Publish Date: June 20, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk allergen Company Name: Sabores Fit Bakery Brand Name: Brand Name(s) Sabores A Tu Mesa Product Description: Product Description Mousse Desserts Company Announcement Sabores Fit Bakery of Kissimmee, FL…
Transderm Scōp (Scopolamine Transdermal System): Drug Safety Communication – FDA Adds Warning About Serious Risk of Heat-Related Complications with Antinausea Patch
AUDIENCE: Patient, Health Care Professional, Neurology ISSUE: The FDA is warning that the antinausea patch Transderm Scōp (scopolamine transdermal system) can increase body temperature and cause heat-related complications, resulting in hospitalization or even death in some cases. Most cases occurred in children 17 years and younger and in adults 60 years and older, who may…
Lipari Foods Issues Allergy Alert on Undeclared Milk in “Dark Chocolate Nonpareils”
Summary Company Announcement Date: June 20, 2025 FDA Publish Date: June 20, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk allergen Company Name: Lipari Foods Brand Name: Brand Name(s) Product Description: Product Description Dark chocolate nonpareils Company Announcement Lipari Foods of Warren, MI, is recalling its 14-ounce packages…
Convenience Kit Recall: Medline Industries, LP, Removes Medline Neonatal and Pediatric Kits containing Smiths Medical ORAL/NASAL Endotracheal Tubes Due to Smaller Than Expected Tube Diameter That May Cause Underventilation
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 Products Product Name Product Code UDI NEONATAL INTUBATION TRAY ACC010371C 10193489268188 NEWBORN RESUSCITATION KIT ACC010381A 10193489800944 …
Blood Products Administration Set Recall: Fresenius Kabi Removes Large Volume Pump Blood Products Administration Sets due to Incorrect Assembly
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 Description Part Number UDI-DI Lot Number LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site,…
Weaver Nut Company Inc., Issues Allergy Alert on Undeclared Milk in Chocolate Nonpareils
Summary Company Announcement Date: June 17, 2025 FDA Publish Date: June 18, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk allergen Company Name: Weaver Nut Company Brand Name: Brand Name(s) Weaver Nut Company Product Description: Product Description Semi sweet chocolate pareils with white or Christmas colored seeds Company…
Medtech Products Inc. Issues Nationwide Recall of Little Remedies® Honey Cough Syrup Due to Microbial Contamination
Summary Company Announcement Date: June 17, 2025 FDA Publish Date: June 18, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Bacillus cereus Company Name: Medtech Products Inc. Brand Name: Brand Name(s) Little Remedies Product Description: Product Description Honey Cough Syrup Company Announcement TARRYTOWN, N.Y.–(GLOBE NEWSWIRE)—June…
Aspiration Catheter Recall: Q’Apel Medical, Inc. Removes Hippo 072 Aspiration System and Cheetah Delivery Tool After FDA Warning Letter About Internal Processes and Distal Tip Characteristics
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 Products Product Names: 072 Aspiration System or Hippo 072 Aspiration System including Cheetah Delivery Tool and…
Meijer Issues Recall on Frederik’s Dark Chocolate Almonds Due to Presence of Undeclared Cashews
Summary Company Announcement Date: June 13, 2025 FDA Publish Date: June 16, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared cashews Company Name: Meijer Brand Name: Brand Name(s) Frederick’s by Meijer Product Description: Product Description Dark Chocolate Almonds Company Announcement GRAND RAPIDS, Mich., June 13, 2025 – Meijer is…