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FDA
January 29, 2025
Wismettac Asian Foods Issues Allergy Alert on Undeclared Milk in Curvee Puffs Corn Puff Snack
Wismettac Asian Foods, Inc., Santa Fe Springs, CA is expanding its January 17, 2025 recall of 2.46 oz packages of…
FDA
January 27, 2025
New York Wholesale Group Recalls Zaarah Herbals Shatavari Powder Because of Possible Health Risk
New York Wholesale Group of Hicksville, NY is recalling Zaarah Herbals Shatavari Powder, to the consumer/user level because it has…
FDA
January 25, 2025
Recall of La Fiesta Brand Bread Crumbs (Unseasoned and Seasoned) for Undeclared Sesame
La Fiesta Food Products, LLC, La Mirada, CA is recalling 8 oz packages of La Fiesta brand Unseasoned Bread Crumbs…
FDA
January 24, 2025
TS Food Packaging is Recalling its “Rural King” and “Wabash Valley Farms” Bacon Seasoning Due to the Presence of an Undeclared Soy Ingredient
TS Food Packaging is recalling its “Rural King” and “Wabash Valley Farms” Bacon Seasoning due to the presence of an…
FDA
January 22, 2025
Copaxone, Glatopa (glatiramer acetate): Drug Safety Communication – FDA Adds Boxed Warning About a Rare but Serious Allergic Reaction Called Anaphylaxis
The FDA is warning about the risk of a rare but serious allergic reaction with the medicine glatiramer acetate (Copaxone,…
FDA
January 21, 2025
D. Coluccio & Sons, Issues Allergy Alert on Undeclared Almonds in “Colussi Cantuccini Chocolate Drops” Cookies
D. COLUCCIO & SONS, in is recalling its 300 gram packages of “Colussi Cantuccini Chocolate Drops” chocolate chip cookies because…
FDA
January 18, 2025
Monkey Spit, LLC Issues Allergy Alert on Undeclared Milk/Wheat/Soy in Monkey Spit BBQ Sauces
People who have allergies to milk/wheat/soy run the risk of serious or life-threatening allergic reaction if they consume these products.…
FDA
January 17, 2025
Wismettac Asian Foods Issues Allergy Alert on Undeclared Milk in Curvee Puffs Corn Puff Snack Curry Flavor
Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 2.46 oz packages of Shirakiku brand Curvee Puffs Corn Puff…
FDA
January 17, 2025
Max Mobility / Permobil Issues Nationwide Recall of SmartDrive Speed Control Dial Due to the Motor Being Unresponsive to the User
Max Mobility/Permobil has initiated a nationwide recall of the Speed Control Dial component used with the SmartDrive MX2+ Power Assist…
FDA
January 16, 2025
Early Alert: Infusion Pump Software Issue from Fresenius Kabi USA
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
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