Summary Company Announcement Date: February 20, 2025 FDA Publish Date: February 20, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared wheat, sesame, soy, yellow 5, yellow 6, red 6 Company Name: Kedake Inc Brand Name: Brand Name(s) Product Description: Product Description Las Ollas Botana Mix Snacks and Delights 2…
ZB Importing Issue Voluntary Recall and Allergy Alert on Undeclared Egg, Wheat and Milk in Certain Ulker Brand Products
Summary Company Announcement Date: February 18, 2025 FDA Publish Date: February 20, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared allergen (wheat, eggs, milk) Company Name: ZB Importing LLC Brand Name: Brand Name(s) Product Description: Product Description Snack rolls, biscuits, and wafers Company Announcement ZB Importing LLC is voluntarily…
Naturipe Value Added Fresh LLC Issues Allergy Alert On Undeclared Wheat & Eggs In “Berry Buddies, Berries & Pancakes” Lot # 1097901
Summary Company Announcement Date: February 18, 2025 FDA Publish Date: February 19, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared allergen (wheat, eggs) Company Name: Naturipe Value Added Fresh LLC Brand Name: Brand Name(s) Naturipe Snacks Product Description: Product Description Berry Buddies, Berries & Pancakes bento box snack packs…
BD Announces Voluntary Worldwide Recall for One Lot of ChloraPrep™ Clear 1 mL Applicators Due to Fungal Contamination
Summary Company Announcement Date: February 15, 2025 FDA Publish Date: February 18, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Potential for fungal contamination under certain environmental conditions allowing the growth of Aspergillus penicillioides Company Name: BD Brand Name: Brand Name(s) Product Description: Product Description ChloraPrep Clear 1 mL applicator skin preparation product…
Heart Pump Recall: Abiomed, Inc. Updates Use Instructions for Impella RP with SmartAssist and Impella RP Flex with SmartAssist Due to A Risk That the Tip of Guidewires or Other Medical Devices May Come into Contact with The Impella Pump During Insertion, Adjustment, Or Removal
This recall involves updating instructions for using 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 following the updated instructions. Affected Product Product…
Mauna Loa Macadamia Nut Company, LLC Issues a Product Recall on Undeclared Almonds in Mauna Loa Milk Chocolate Covered Macadamias (1oz) Pouches
Summary Company Announcement Date: February 15, 2025 FDA Publish Date: February 15, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared almonds Company Name: Mauna Loa Macadamia Nut Company, LLC Brand Name: Brand Name(s) Product Description: Product Description Mauna Loa Milk Chocolate Covered Macadamias Company Announcement February 15, 2025, Mauna Loa…
JE Bakery 2019 LLC DBA Broadway Bakery Issues Allergy Alert for Mislabeled Raisin Bran Muffin 6 Count Due to Undeclared Walnuts
Summary Company Announcement Date: February 13, 2025 FDA Publish Date: February 14, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared walnuts Company Name: JE Bakery LLC DBA Broadway Bakery Brand Name: Brand Name(s) Cub Foods, Jerrys Foods, Country Market Product Description: Product Description Raisin Bran Muffin Company Announcement JE Bakery…
ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and Potassium Chloride Injection, 10 mEq Due to Mislabeling
Summary Company Announcement Date: February 13, 2025 FDA Publish Date: February 14, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Bags of POTASSIUM CHLORIDE Inj. 20 mEq have incorrect overwrap labels which state POTASSIUM CHLORIDE Inj. 10 mEq. Company Name: ICU Medical Brand Name: Brand Name(s) ICU Medical Product Description: Product Description POTASSIUM…
Glucose and Glucose/Ketone Meter Correction: Nova Biomedical Corporation Issues Software Correction for StatStrip Glucose and Glucose/Ketone Hospital Meters Due to Risk for Transmission of Incorrect Patient Results
This recall involves correcting 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 StatStrip Glucose Hospital Meter System StatStrip…
AKT Trading Inc. Recalls Seasoned Bamboo Shoots Because of Possible Health Risk
Summary Company Announcement Date: February 11, 2025 FDA Publish Date: February 12, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Botulism Company Name: AKT Trading Inc. Brand Name: Brand Name(s) Product Description: Product Description Menma Ajitsuke Prepared Bamboo Shoot Company Announcement AKT Trading Inc of…