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U.S. FDA Recalls @FDArecalls

Our tweets are FDA Approved! Get notified about the U.S. Food and Drug Administration's recalls. Privacy Policy - https://t.co/AUq6FZaMu1 fda.gov/Safety/Recalls… Washington, DC Joined December 2008
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U.S. FDA Recalls retweeted
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FDA FOOD (Ctr for Food Safety & Applied Nutrition) @FDAfood

2 days ago

FDA advises restaurants & retailers not to sell and consumers not to eat certain frozen, raw, half-shell oysters from Republic of Korea potentially contaminated with norovirus fda.gov/food/alerts-ad…

U.S. FDA Recalls retweeted
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FDA FOOD (Ctr for Food Safety & Applied Nutrition) @FDAfood

21 hours ago

Multistate #outbreak of Salmonella linked to Infinite Herbs-brand organic basil previously sold at Trader Joe’s stores in 29 states and DC. Product has been removed from store shelves. Learn more at: fda.gov/food/outbreaks…

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U.S. FDA Recalls @FDArecalls

3 days ago

Cargill Conducts Voluntary Recall of Nutrena® Country Feeds® Meatbird 22% Crumble Due to Non-inclusion of Vitamin D fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

3 days ago

Gracie’s Kitchen Inc. Issues Allergy Alert on Undeclared Sesame and Wheat Allergens in “Broccoli Cutlets” fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

3 days ago

Roly Poly Bakery Issues Allergy Alert on Undeclared Egg Ingredient in Multigrain Bread fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

3 days ago

Feel Good Foods Issues Voluntary Recall of Gluten-Free Cream Cheese Stuffed Mini Bagels fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

6 days ago

ADM Animal Nutrition Expands Recall to Include 17 Additional Lots of Chicken, Swine and Rabbit Feed Products fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Global Mix, Inc Recalls Tejocote Products Because of Possible Health Risk fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Home Style Foods, Inc. Issues Allergy Alert on Undeclared Egg in Kowalski Simply Sides – Jack’s Potato Salad fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Oregon Spice Company Issues Allergy Alert on Undeclared Sesame in Johnny’s Parmesan Garlic Seasoning fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Baron Spices, Inc. Issues Allergy Alert on Undeclared Soy and Wheat in Blues Hog Sweet & Savory Seasoning fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Belgian Yummies Issues Allergy Alert on Undeclared Allergens of Wheat, Soy, Egg, Coconut and/or Peanuts and FD&C Yellow #5 in Ice Cream Sandwiches and Gelato fda.gov/safety/recalls…

U.S. FDA Recalls retweeted
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CDC @CDCgov

a week ago

LISTERIA OUTBREAK linked to queso fresco and cotija cheese is over. Recalled foods are no longer within shelf life. Share this info with family and friends, and stay up-to-date on recalls. bit.ly/3Oy0gVU

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U.S. FDA Recalls @FDArecalls

a week ago

Medline Industries, LP Issues a Nationwide Recall of Convenience Kits Containing Nurse Assist 0.9% Sodium Chloride Irrigation USP and Sterile Water for Irrigation USP fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Aruba Aloe Balm N.V. Issues Voluntary Nationwide Recall of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel Due to Presence of Methanol fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

a week ago

Honeywell Safety Products USA, Inc. Issues Voluntary Worldwide Recall of Honeywell Fendall 2000 Non-Sterile Eyewash Cartridges # 32-002050-0000 used with the Fendall 2000 Eyewash Station Due to a Lack of Appropriate Policies and Procedures by Honeywell’s Supplier…

U.S. FDA Recalls retweeted
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FDA Medical Devices @FDADeviceInfo

2 weeks ago

The @US_FDA has identified a Class I Recall, the most serious type of recall: Smiths Medical ASD recalls PneuPac ParaPAC Plus 300 and 310 ventilator kits for a malfunction causing non-cycling, continuous positive gas flow and preventing proper ventilation fda.gov/medical-device…

U.S. FDA Recalls retweeted
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FDA Medical Devices @FDADeviceInfo

2 weeks ago

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Medos International Sàrl is recalling the Cerenovus CEREBASE DA Guide Sheath due to complaints describing fractures of the distal catheter shaft. Find out more: fda.gov/medical-device…

U.S. FDA Recalls retweeted
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US FDA MedWatch @FDAMedWatch

2 weeks ago

ForeverMen by FAonline: Recall - Due Presence of Sildenafil and Tadalafil fda.gov/safety/recalls…

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U.S. FDA Recalls @FDArecalls

2 weeks ago

World Green Nutrition, Inc. Announces Expansion of Recall of Tejocote Products Due to the Presence of Yellow Oleander fda.gov/safety/recalls…

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