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…
Fuentes Farms, LLC Recalls Product Because of Possible Health Risk
Summary Company Announcement Date: June 13, 2025 FDA Publish Date: June 16, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Fuentes Farms Inc. Brand Name: Brand Name(s) Fuentes Farms Inc Product Description: Product Description Cucumbers in bushel boxes Company Announcement Fuentes Farms…
Infusion Pump Recall: Zyno Medical Removes Certain Z-800 Series Infusion Pumps due to Software Issue
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 Affected Serial Numbers for Z-800 (UDI-DI: 00814377102006) 800242 801925 802867 900875 901058 901089 901101 901126…
Intra-Operative Positioning System Guidewire Recall: Centerline Biomedical Removes Certain IOPS Guidewires due to Delamination
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 Device Name Model Number UDI-DI Lot Number IOPS Guidewire ATW-2 H01035 00843152102051 2404-2005 What to…
Vita-Warehouse Corp. Issues Allergy Alert on Undeclared Peanut Allergen in ALDI Welby®, Berkley Jensen®, and VitaGlobe™ Vitamin B12 Gummy Products
Summary Company Announcement Date: June 12, 2025 FDA Publish Date: June 13, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared allergen – peanut Company Name: Vita Warehouse Corp. Brand Name: Brand Name(s) Welby, Berkely Jensen and VitaGlobe Product Description: Product Description Gummy products Company Announcement Company Announcement: June 12,…
Liquid Bicarbonate Concentrate Recall: Nipro Removes MedicaLyte Liquid Bicarbonate Concentrate due to Contamination
This recall involves removing 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 MedicaLyte Liquid Bicarbonate Concentrate – 45x Proportioning (BC+201) Unique Device Identifier (UDI)/Model: 00817411022824 What to Do…