Image Español If you’re bothered by bumps on your skin, don’t try to diagnose yourself or treat your condition with products that haven’t been approved by the U.S. Food and Drug Administration. Instead, visit a health care professional for a proper diagnosis and to make a treatment plan. One common condition that some people try…
Twin City Foods, Inc., Recalls Frozen Super Sweet Corn and Mixed Vegetables Because of Possible Health Risk
Product Name UPC Lot and Best if Used By Date FOOD LION Mixed Vegetables Carrots, Corn, GreenBeans & Peas, net wt. 16oz 35826005090 50183 BEST BY 18 JAN 2025 PROD OF USA FOOD LION Super Sweet Cut Yellow Corn, net wt. 16oz. 35826079855 53072 BEST BY 03 NOV 2024 PROD OF USA FOOD LION Super…
Datascope/Maquet/Getinge Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for PCBA Failures Affecting the Ability to Charge the Batteries Leading to Unexpected Shutdowns
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Names: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Product Models: Distribution Dates: March 6, 2012 to May 19, 2023 Devices…
Abiomed Recalls the Labeling for Impella RP Flex with SmartAssist for Risk of Blood Clots
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Please be aware, this recall is a voluntary correction, not a product removal. Recalled Product Product Names: Impella RP Flex with SmartAssist Product Codes: See Recall Database Entry Model…
Philips Respironics Recalls Trilogy Evo, Evo O2, EV300, and Evo Universal Ventilators After Finding Dust and Dirt in Air Path That Can Reduce Air Flow to Patients
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: Philips Respironics Trilogy Evo, Trilogy Evo O2, Trilogy EV300, Trilogy Evo Universal Product Models and Serial Numbers: See Medical Device Recall Database Distribution Dates: March…
Stonewall Kitchen Issues Allergy Alert on Undeclared Soy, Wheat, and Peanuts in Peanut Butter Maltballs (6oz.)
Summary Company Announcement Date: August 14, 2023 FDA Publish Date: August 14, 2023 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared soy, wheat, peanut allergens Company Name: Stonewall Kitchen Brand Name: Brand Name(s) Stonewall Kitchen Product Description: Product Description Peanut Butter Maltballs Company Announcement Stonewall Kitchen of York, Maine is…
Nestlé USA Announces Voluntary Recall of Limited Quantity of NESTLÉ® TOLL HOUSE® Chocolate Chip Cookie Dough Bar (16.5 Oz) Due to Potential Presence of Foreign Material
Summary Company Announcement Date: August 10, 2023 FDA Publish Date: August 11, 2023 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential presence of wood fragments Company Name: Nestle USA Brand Name: Brand Name(s) NESTLÉ® TOLL HOUSE® Product Description: Product Description Chocolate Chip Cookie Dough Company Announcement ARLINGTON, VA., August 10, 2023…
Do Not Use Tests Manufactured by Universal Meditech, Inc.: FDA Safety Communication
Date Issued: August 11, 2023 The U.S. Food and Drug Administration (FDA) is warning consumers and patients to not use the following tests manufactured by Universal Meditech, Inc. (UMI): One Step Pregnancy Test DiagnosUS One Step Ovulation Test HealthyWiser UriTest 10 Parameter Reagent Test Strips for Urinalysis HealthyWiser UriTest UTI Test Strips HealthyWiser KetoFast Ketone…
Unilever U.S. Voluntarily Recalls Select Knorr Sopa Soup Mix Products Due to Potential Undeclared Egg Allergen
Summary Company Announcement Date: August 10, 2023 FDA Publish Date: August 10, 2023 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared egg Company Name: Unilever United States Inc. Brand Name: Brand Name(s) Product Description: Product Description Knorr Sopa Soup Mix products Company Announcement FOR IMMEDIATE RELEASE – Englewood Cliffs, New…
Datascope/Maquet/Getinge Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for Unexpected Shutdowns
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Recalled Product: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Product Models: Distribution Dates: March 6, 2012 to May 19, 2023 Devices…