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U.S. FDA Jan 24
Savannah Food Company, Inc. Voluntarily Recalls Cornbread Dressing and Bread Stuffing Products Due to Possible Health Risk
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U.S. FDA Jan 23
ABH NATURE’S PRODUCTS, INC, ABH PHARMA, INC., and , INC. Issues Nationwide Recall of All Lots of Dietary Supplement Products
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U.S. FDA Jan 23
Five Star Food Recalls Sham Gardens Excellent Tahina Because of Possible Health Risk
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U.S. FDA Jan 23
Lipari Foods Issues Voluntary Recall Expansion on Additional Sandwiches Due to Potential Contamination of Listeria Monocytogenes
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U.S. FDA Jan 22
Five Star Food Recalls Sham Gardens Excellent Tahina Because of Possible Health Risk
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U.S. FDA Jan 17
FUSION IV Pharmaceuticals, Inc dba. AXIA Pharmaceutical Issues Voluntary Nationwide Recall of All Sterile Drug Products Within Expiry Due to A Lack of Assurance of Sterility
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U.S. FDA Jan 17
Yes To Inc. Issues Voluntary Recall of Product Due to Skin Irritation Complaints ‘Grapefruit Vitamin C Glow Boosting Unicorn Paper Mask’
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U.S. FDA Jan 14
Lipari Foods Issues Voluntary Recall Expansion on Additional Sandwiches Due to Potential Contamination of Listeria Monocytogenes
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U.S. FDA Jan 13
Taro Pharmaceuticals U.S.A., Inc. Issues Voluntary Nationwide Recall of Lamotrigine Tablets USP, 100 mg, 100 Count Bottles
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U.S. FDA Jan 10
Stryker Launches Voluntary Field Action for Specific Units of The LIFEPAK® 15 Monitor/Defibrillator
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U.S. FDA Jan 9
Mavidon Issues Voluntary Worldwide Recall of Manufactured Products Including Lemonprep® Tubes And Single Use Cups Pediaprep® Tubes And Single Use Cups Wave Prep® Tubes & Single Use Cups Cardio Prep Single Use Cups Due To Burkholderia Cepacia Contamination
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U.S. FDA Jan 9
Mylan Initiates Voluntary Nationwide Recall of 3 Lots of Nizatidine Capsules, USP, Due to Trace Amounts of NDMA (N-Nitrosodimethylamine) Impurity Found in the Active Pharmaceutical Ingredient Manufactured by Solara Active Pharma Sciences Limited
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U.S. FDA Jan 8
Fresh Location Announces Product Recall Due to Possible Listeria Contamination
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U.S. FDA Jan 8
Denton Pharma, Inc. dba Northwind Pharmaceuticals Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity
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U.S. FDA Jan 8
Appco Pharma LLC Issues Voluntary Nationwide Recall of Ranitidine Hydrochloride Capsules 150 mg and 300 mg Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA)
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U.S. FDA Jan 6
Jeni’s Splendid Ice Creams Issues Voluntary Recall of Cold Brew with Coconut Cream
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U.S. FDA Jan 6
Purely Elizabeth Recalls Pouches of Chocolate Sea Salt Probiotic Granola Recall Due to a Mislabeling Error That Has Resulted in an Undeclared Allergen
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U.S. FDA Jan 6
Ducktrap River of Maine Recalls One Lot of Herring Center Cuts in Wine Sauce Due to Undeclared Dairy in Product
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U.S. FDA Jan 3
Cargill Voluntarily Recalls 39 One-Pound Bags of Product Packaged as Wilbur Dark Chocolate Covered Cashews; Wheat Allergen Presence
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U.S. FDA Jan 2
Limena, LLC Recalls "Salvadorean String Cheese (Quesillo Cheese)" Because of Possible Health Risk
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