Summary Company Announcement Date: July 30, 2025 FDA Publish Date: July 31, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Doehler Dry Ingredient Solutions, LLC Brand Name: Brand Name(s) Member’s Mark Product Description: Product Description Freeze dried fruit Company Announcement Cartersville,…
Products Containing 7-OH Can Cause Serious Harm
Image Products Containing 7-OH Can Cause Serious Harm Tempted to try products containing 7-hydroxymitragynine (also known as 7-OH) – such as tablets, gummies, drink mixes, and shots – sold online and at smoke shops and gas stations? Consider this: 7-OH products are novel potent opioid products that have not been proven safe or effective for…
Albertsons Companies Stores in Arkansas, Louisiana, Oklahoma and Texas Voluntarily Expands Recall to Select Items Containing Tuna Salad from Reser’s Fine Foods Due to an Ingredient Recall Linked to Possible Listeria monocytogenes Contamination
Summary Company Announcement Date: July 26, 2025 FDA Publish Date: July 28, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Albertsons Brand Name: Brand Name(s) Randalls, Albertsons, Tom Thumb Product Description: Product Description Additional Tuna Salad products Company Announcement Albertsons, Randalls…
Hillside Orchard Farms Recalls Various Fruit Breads & Fritters Due to Undeclared Egg
Summary Company Announcement Date: July 28, 2025 FDA Publish Date: July 28, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Allergen – Egg Company Name: Hillside Orchard Farms Brand Name: Brand Name(s) Hillside Orchard Farms Product Description: Product Description Fruit Bread and Fritters Company Announcement Tiger GA – July…
Cranial Drill Recall: Integra LifeSciences Recalls Codman Disposable Perforators Due to Risk of Device Disassembly
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 Name Unique Device Identifier (UDI) Codman Disposable Perforator 14 mm 10381780513599 Codman Craniotomy Kit…
Tropicale Foods Recalls Certain Helados Mexico and La Michoacana Products Due to Undeclared Milk
Summary Company Announcement Date: July 25, 2025 FDA Publish Date: July 26, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Tropicale Foods Brand Name: Brand Name(s) La Michoacana, Helados Mexico Product Description: Product Description Ice cream products Company Announcement Tropicale Foods of Ontario, CA is recalling certain…
Continuous Ventilator (Respirator) Correction: Maquet Critical Care AB Updates Use Instructions for Servo Ventilator Systems Due to Risk of Inaccurate Compliance Measurement Leading to Improper Tidal Volume Delivery in Neonatal Patients
This recall involves updating instructions for using 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 following the updated instructions. Affected Product Product Names:…
Medical Procedure Kits Correction: Medline Industries, LP Issues Correction for Medline Craniotomy Kits Containing Codman Disposable Perforators Due to Risk for Device Disassembly
Craniotomy Kit DYNJ35349C 10888277858060 (EA), 40888277858061 (CASE) 24CBJ925, 24DBT405, 24FBO318 CRANI Accessory Pack DYNJ59270 10888277771512 (EA), 40888277771513 (CASE) 23JDB683, 23JDC548, 24ADB783, 24HDA822 CRANI PACK-LF DYNJ44805M 10195327506872 (EA), 40195327506873 (CASE) 23JBI747, 23KBL228, 24ABG696, 24CBM117, 24EBQ114, 24GBJ699 CRANIOTOMY KIT CDS982719V 10195327510831 (EA), 40195327510832 (CASE) 23KBP461, 23LBN381, 24ABB119, 24BBC547, 24BBI145 CRANIOTOMY KIT CDS982719W 10195327645090 (EA), 40195327645091 (CASE) 24DBS813…
Disposable Surgical Stapler Cartridge Correction: Ethicon Endo-Surgery, LLC Issues Correction for Endopath Echelon to Address Inadvertent Lockout During Surgical Procedures
This recall involve correcting certain 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 Names: Endopath Echelon Vascular White Reload…
Arterial Cannula Recall: Edwards Lifesciences Removes Arterial Cannula due to Risk of Wire Exposure
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 Product Family Model Number UDI-DI OptiSite Arterial Perfusion Cannula OPTI16 00690103180558 OptiSite Arterial Perfusion Cannula OPTI18…