Velvet Ice Cream Recalls Various Products Due to Possible Listeria Risk

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Velvet Ice Cream has announced it is voluntarily recalling all of its ice cream and sherbet products made on or after March 24, 2021 as a precaution because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in y

Source: FDA Food Safety Recalls RSS Feed

Wolfies Roasted Nut Co. Issues Voluntary Recall of its Crunchy Cheddar & Jalapeno Nuts

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Wolfies Roasted Nut Co. in Findlay, Ohio is voluntarily recalling its Crunchy Cheddar & Jalapeno Nuts due to an undeclared milk allergen. This recall has been initiated due to the ingredient label not stating a milk allergen. Products were packaged in either a 5 oz, 14 oz, 28 oz black rice paper s

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

Golden Medal Mushroom Inc. Recalls Enoki Mushrooms Because of Possible Health Risk

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Golden Medal Mushroom Inc. of Los Angeles, CA is recalling all cases of its 200g/7.05-ounce packages of Enoki Mushrooms (Product of Korea) because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children

Source: FDA Food Safety Recalls RSS Feed

Jule’s Foods Issues Voluntary Recall of Jule’s Foods Products Because of Possible Health Risk

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Jule’s Foods of Carlsbad, CA is voluntarily recalling all Jule’s Foods products, because the product was potentially contaminated with Salmonella.

Source: FDA Food Safety Recalls RSS Feed

Faribault Foods, Inc. Announces Voluntary Recall of a Limited Quantity of S&W Brand Organic Black Beans, and O Organic Brand Black Beans and O Organic Brand Chili Beans Due to Compromised Hermetic Seal

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Faribault Foods, Inc. is voluntarily recalling 15 ounce cans of S&W Organic Black Beans, 15 ounce cans of O Organic Brand Black Beans and 15 ounce cans of O Organic Brand Chili Beans because the cans may have a compromised hermetic seal. The compromised hermetic seal may affect can integrity and ma

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

Guan’s Mushroom Co Recalls Enoki Because of Possible Health Risk

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Guan’s Mushroom Co of Commerce, CA is recalling all cases of its 200g/7.05-ounce packages of Enoki Mushroom (Product of China) because it has the potential to be contaminated with Listeria monocytogenes

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

Guan’s Mushroom Co Recalls Enoki Because of Possible Health Risk

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Guan’s Mushroom Co of Commerce, CA is recalling all cases of its 200g/7.05-ounce packages of Enoki Mushroom (Product of China) because it has the potential to be contaminated with Listeria monocytogenes

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

BD Announces the Voluntary Recall of Specified Lots of ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator in the United States and U.S. Territories Due to Defective Applicator

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BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily recalling specified lots of the ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator (2% w/w chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) to the user level due to a defective applicator.

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

Church & Dwight Initiates Voluntary Recall of Select Vitamins Due to Isolated Manufacturing Issue

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EWING, N.J – Church & Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of select vitafusion gummy products after the Company’s investigation of two consumer reports identified the possible presence of a metallic mesh material in product lots manufactured in a four-day period between Oc

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

Tenacore LLC Issues Nationwide Recall of Tenacore’s Replacement for the Front Bezel Assembly of the CareFusion Alaris 8100 Infusion Pump Module

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On February 24th, 2021, Tenacore LLC initiated a nationwide recall of 2001 Tenacore replacement CareFusion Alaris 8100 bezels due to potentially weakened plastic. A bezel with weakened plastic may, over time, lead to separation of the bezel post (recall issue) as well as other damage to the bezel (e

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