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FDA
May 2, 2025
Williams Farms Repack LLC Recalls Tomatoes Due to Possible Salmonella Contamination
Williams Farms Repack LLC is recalling Tomatoes sizes; 4×5 2 layer, 60ct 2layer, 3ct trays in the Williams Farms Repack…
FDA
May 1, 2025
East Trading Inc., Issues Alert on Undeclared Sulfites in “Licorice Plum”
East CK Trading, Inc. of Long Island City, NY, is recalling its 8-ounce packages of “Licorice Plum” food treats because…
FDA
April 28, 2025
Food Co. Issues Allergy Alert on Undeclared Milk in Monkfish Liver – Ankimo
JJWV Marketing Corporation of Santa Fe Springs, California is recalling Ankimo Monkfish Liver because it may contain undeclared milk. People…
FDA
April 28, 2025
Trader Joe’s Sesame Miso Salad with Salmon Voluntarily Recalled Due to Undeclared Milk Allergen
FOR IMMEDIATE RELEASE – April 28, 2025 – A limited quantity of Trader Joe’s Sesame Miso Salad with Salmon is…
FDA
April 26, 2025
Mauna Loa Macadamia Nut Company, LLC Issues Allergy Alert on Undeclared Almonds and Cashews in Mauna Loa Dark Chocolate Covered Macadamias (0.6OZ and 4OZ)
Mauna Loa Macadamia Nut Company LLC of Kea’au, HI is voluntarily recalling Mauna Loa Dark Chocolate Covered Macadamias (0.6oz and…
FDA
April 25, 2025
Health Fixer Issues Voluntary Nationwide Recall of Male Ultra, Malextra, Electro Buzz, Ultra Armor and Male Ultra Pro Due to Undeclared Chloropretadalafil, Propoxyphenylsildenafil and Sildenafil
Tempe, AZ, HEALTH FIXER is voluntarily recalling all lots of dietary supplements by the name of Male Ultra, Malextra, Electro…
FDA
April 25, 2025
My Life Inc Issues Allergy Alert on Undeclared Milk in ML Natural Premium Quality Lactoferrin as Apolactoferrin
April 25, 2025, My Life Inc. of Federal Way, WA is recalling approximately 65 bottles of ML Naturals Premium Quality…
FDA
April 24, 2025
New England Village Foods Issues Allergy Alert on Undeclared Almonds in “19th Hole Snack Mix”
New England Village Foods of Milford NH is recalling all lots of 5 -ounce and 10 -ounce containers of New…
FDA
April 24, 2025
Heart Pump Accessory Removal: Abbott Removes HeartMate Mobile Power Unit due to Instances of Sudden Power Loss
Heart Pump Accessory Removal: Abbott Removes HeartMate Mobile Power Unit due to Instances of Sudden Power Loss
FDA
April 24, 2025
Risk of False Positive Results with Certain Capillary Blood Collection Tubes Used with Magellan Diagnostics LeadCare Testing Systems – FDA Safety Communication
FDA is alerting health care providers and lab staff of reports of false positives when using certain Micro Capillary Blood…
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