Summary Company Announcement Date: April 02, 2025 FDA Publish Date: April 02, 2025 Product Type: Food & Beverages Bakery Product/Mix Allergens Reason for Announcement: Recall Reason Description May contain undeclared milk Company Name: Panaderia Salvadorena Inc. Brand Name: Brand Name(s) Panaderia/Bakery Product Description: Product Description Quesadilla de Queso bread Company Announcement Panaderia Salvadorena Inc., of…
Vascular Cannula Recall: Medtronic Removes Aortic Root Cannula Due to Unexpected Loose Material in the Male Luer
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 Names: DLP Aortic Root Cannula MiAR Cannula DLP Aortic Root Cannula with Vent Line…
Undeclared Allergen in Trader Joe’s Hot Honey Mustard Dressing with Use By Date of 05/27/2025 Issued by Fresh Creative Foods
Summary Company Announcement Date: March 30, 2025 FDA Publish Date: March 31, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared allergen – peanut, soy, sesame, and wheat. Company Name: Fresh Creative Foods Brand Name: Brand Name(s) Trader Joe’s Product Description: Product Description Hot honey mustard dressing Company Announcement Vista,…
The Bakery Group Issues Allergen Alert on Undeclared Milk, Soy and Yellow FD&C #5 In Specific Bread and Hamburger Buns
Summary Company Announcement Date: March 25, 2025 FDA Publish Date: March 28, 2025 Product Type: Food & Beverages Bakery Product/Mix Allergens Reason for Announcement: Recall Reason Description May contain undeclared milk, soy and yellow FD&C # 5 Company Name: The Bakery Group Brand Name: Brand Name(s) Ben E. Keith, Rodeo Goat, Casa Linda Product Description:…
Cromer Food Services, Inc. Recalls Chicken Salad on White Sandwich Due to Undeclared Milk Allergen
Summary Company Announcement Date: March 27, 2025 FDA Publish Date: March 27, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Cromer Food Services, Inc. Brand Name: Brand Name(s) CFS Cromer Food Services, Inc. Product Description: Product Description Chicken salad on white bread sandwich Company Announcement Cromer Food…
Frito-Lay Issues Limited Recall for Tostitos Cantina Traditional Yellow Corn Tortilla Chips for Undeclared Milk
Summary Company Announcement Date: March 26, 2025 FDA Publish Date: March 27, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Frito-Lay Brand Name: Brand Name(s) Product Description: Product Description Cantina Traditional Yellow Corn Tortilla Chips Company Announcement Frito-Lay today issued a recall of a limited number of…
Safe Use of Megadyne Mega 2000 and Mega Soft Patient Return Electrodes – Letter to Health Care Providers
UPDATE: March 2025 The FDA is providing an update that Megadyne has communicated in a letter the availability of a labeling (pad printing) update for Megadyne Mega Soft Universal (0845 & 0846) and Universal Plus (0847 & 0848) Reusable Patient Return Electrodes. The pad printing will now show the updated indication which is for patients…
Pulse Oximeter Basics
Image Español中文한국의TagalogTiếng Việt We need oxygen to survive. Sometimes the amount of oxygen in the blood falls too low for the body to function well. Asthma, lung cancer, chronic obstructive pulmonary disease, the flu, and heart disease are among the health conditions that can cause oxygen levels to drop. Being at higher altitudes, where the…
Endotracheal Tube Recall: Smiths Medical Removes Intubation 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 Product Product Name Product Code UDI TRACHEAL TUBE SILICONISED ORAL/NASAL UNCUFFED 2.5MM 10/BX 100/111/025 15019315018848 TRACHEAL…
Implantable Port Recall: Smiths Medical Removes ProPort Plastic Implantable Ports Due to Manufacturing Error that May Cause Separation
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 Item Number Product Name and Description UDI 21-4153-24 ProPort (Plastic standard portal) 1.9 mm PUR…