Veata LLC Issues Voluntary Nationwide Recall of Endurance Pro Capsules Due to the Potential Presence of Undeclared Sildenafil

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Sacramento CA, Veata LLC is voluntarily recalling lot 230811, Exp 8/11/25 of Endurance Pro Energy Boost capsules, packaged in 10-count blisters ina cardboard carton to the consumer level. Veata LLC was notified by Amazon that the products were found to be tainted with sildenafil, an ingredient in FD

Source: Food and Drugs Administration--Recalls/Safety Alerts

Smiths Medical Issues Urgent Medical Device Notification Informing Customers of a Potential Issue with Certain Bivona® Tracheostomy Tubes

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Smiths Medical issued an Urgent Medical Device Notification on May 29, 2024, to notify affected customers of a potential issue with certain Bivona® Tracheostomy Tubes

Source: Food and Drugs Administration--Recalls/Safety Alerts

Gutierrez Distributor Recalls El Servidor Corp Ground Cinnamon Because of Possible Health Risk

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Gutierrez Distributor of Passaic, NJ is recalling El Servidor Corp brand ground cinnamon because it has the potential to be contaminated with elevated levels of lead. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that increased blood lead levels may be t

Source: FDA Food Safety Recalls RSS Feed

Flagstone Foods, LLC. Allergy Alert on Undeclared Peanuts, Almonds and Pecan in Emerald Kettle Glazed Walnuts

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Flagstone Foods, LLC., manufacturer of Emerald Nuts, is issuing a voluntary recall of 6.5oz Emerald Kettle Glazed Walnut lot 2EE06284 because packages contain undeclared Peanuts, Almonds and Pecans. People who have an allergy or severe sensitivity to Peanuts, Almonds, and Pecans run the risk of ser

Source: FDA Food Safety Recalls RSS Feed

El Chilar HF, LLC. Expands Recall of El Chilar Ground Cinnamon Due to Elevated Levels of Lead

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El Chilar HF, LLC on 03/06/2024 issued a recall of Lots # D-300 EX1024 and F272 EX1026, contained in 127 boxes (12 bags/box) of El Chilar “Cinnamon Ground” (1.25 oz bag), because it may contain traces of lead. Further investigation indicates that the issue could be caused by a potentially adulterate

Source: Food and Drugs Administration--Recalls/Safety Alerts

Tandem Diabetes Care Provides Update on March 2024 Nationwide Recall of t:connect Mobile App for iOS Devices

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Tandem Diabetes Care, Inc. (Nasdaq: TNDM) today provided an update on the March 2024 recall of its Apple iOS t:connect mobile app in the United States relating to an issue that can cause rapid depletion of a user’s t:slim X2 insulin pump battery. This battery depletion can result in the pump shuttin

Source: Food and Drugs Administration--Recalls/Safety Alerts

Tandem Diabetes Care Provides Update on March 2024 Nationwide Recall of t:connect Mobile App for iOS Devices

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Tandem Diabetes Care, Inc. (Nasdaq: TNDM) today provided an update on the March 2024 recall of its Apple iOS t:connect mobile app in the United States relating to an issue that can cause rapid depletion of a user’s t:slim X2 insulin pump battery. This battery depletion can result in the pump shuttin

Source: Food and Drugs Administration--Recalls/Safety Alerts

Prime Food Processing LLC Issues Allergy Alert on Undeclared Sesame in Steam Buns with Egg Custard Added and Steam Buns with Egg Custard and Coconut Added

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Prime Foods Processing LLC of Brooklyn, NY is recalling 477 cases of 2 varieties of Egg Custard Steamed Buns because they may contain undeclared Sesame. People who have an allergy or severe sensitivity to Sesame run the risk of serious or life-threatening allergic reaction if they consume these prod

Source: Food and Drugs Administration--Recalls/Safety Alerts

Prime Food Processing LLC Issues Allergy Alert on Undeclared Sesame in Steam Buns with Egg Custard Added and Steam Buns with Egg Custard and Coconut Added

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Prime Foods Processing LLC of Brooklyn, NY is recalling 477 cases of 2 varieties of Egg Custard Steamed Buns because they may contain undeclared Sesame. People who have an allergy or severe sensitivity to Sesame run the risk of serious or life-threatening allergic reaction if they consume these prod

Source: Food and Drugs Administration--Recalls/Safety Alerts

Breas Medical Issues Voluntary U.S. Nationwide Urgent Medical Device Correction of Vivo 45 LS Ventilator

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On August 5, 2024, Breas Medical initiated a U.S. nationwide correction of 8,186 Vivo 45 LS ventilator devices. Internal testing of the ventilator identified the potential for short term elevated levels of formaldehyde exposure to users under specific conditions. Short term formaldehyde emissions m

Source: Food and Drugs Administration--Recalls/Safety Alerts