Food and Drugs Administration--Recalls/Safety Alerts

Hearty Acquisitions Llc Issues Allergy Alert on Undeclared Soy in Tomato Basil with Rice Exp 3/22/2024

FDA — Thu, 01 Feb 2024 16:12:00 EST

Hearty Acquisitions Inc. of Brooklyn, NY, is recalling its pints of "Tomato Basil with Rice EXP 3/22/2024" 16 Oz containers because they contain Butternut Squash Bisque resulting in soy being undeclared on the label. People who have allergies to soy run the risk of serious or life-threatening allerg

Nam & Son of MD Recalls Soybean Sprouts Because of Possible Health Risk

FDA — Thu, 01 Feb 2024 12:03:00 EST

Nam & Son of MD, Jessup, MD is recalling one-pound bags of soybean sprouts, with the sell-by date of December 21, 2023, because it has the potential to be contaminated with Listeria monocytogenes.

Update: Quaker Issues Revised Recall Notice With Additional Product Due to Possible Health Risk

FDA — Wed, 31 Jan 2024 12:44:00 EST

The Quaker Oats Company today announced an expansion of the December 15, 2023, recall to include additional cereals, bars and snacks listed below because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children,

Byrne Dairy Recalls Mighty Fine Chocolate Ice Cream in Half Gallons Dated 10/4/2024 Due to Undeclared Peanuts

FDA — Tue, 30 Jan 2024 11:11:00 EST

Byrne Dairy, Inc. of Syracuse, New York is voluntarily recalling its Byrne Dairy Mighty Fine Chocolate Ice Cream in half gallon cartons with a Last Date of Sale of 10/4/2024 because it may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening al

Truong Giang Distributor Corp Issues Allergy Alert on Undeclared Sulfites in Dried Mango

FDA — Mon, 29 Jan 2024 00:00:00 EST

TRUONG GIANG DISTRIBUTOR CORP of Philadelphia, PA is recalling Golden Owl Dried Mango, because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume these products. Product was d

Neptune Resources, LLC Issues Voluntary Nationwide Recall of Neptune’s Fix

FDA — Sun, 28 Jan 2024 00:00:00 EST

Neptune Resources, LLC is voluntarily recalling All lots of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets to the consumer level. Neptune Resources LLC's distribution channels have not reported any adverse events from the use of its products. The products are be

Utz Quality Foods Issues Allergy Alert on Undeclared Milk in Utz® Wavy Original Potato Chips in Metro New York Area

FDA — Thu, 25 Jan 2024 00:00:00 EST

Utz Quality Foods, LLC., is issuing a voluntary recall for 88 cases of Utz® 2.75 oz. Wavy Original Potato Chips due to an undeclared milk allergen. This recall was initiated after Utz learned that approximately 1200 single-serve bags contained Utz® Wavy Original Potato Chips flavored with seasoning

Haleon Issues Voluntary Nationwide Recall of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult Products Due to Microbial Contamination

FDA — Wed, 24 Jan 2024 00:00:00 EST

Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult to the consumer level. The product is being recalled due to microbial contamination. In immunocompromised individuals, the use of the affected product could potentially result

Azurity Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Zenzedi® (dextroamphetamine sulfate tablets, USP) 30 mg Due to a Mislabeled Package During Manufacturing

FDA — Wed, 24 Jan 2024 00:00:00 EST

Woburn, Massachusetts, Azurity Pharmaceuticals, Inc. is voluntarily recalling one (1) lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist in Nebraska who opened a bottle of Zenzedi® 30 m

Windstone Medical Packaging dba Aligned Medical Solutions Issues Nationwide Recall of Nurse Assist Sterile Saline Placed Into the Following Kits; AMS10833 Local Lower Extremity Pack I, AMS12947 In House Ocular Pack, AMS12947A In House Ocular Pack and AMS13043 Closure Kit

FDA — Mon, 22 Jan 2024 00:00:00 EST

On December 22, 2023, Aligned Medical Solutions, Billings, MT, initiated a nationwide recall of Nurse Assist Sterile Saline packaged into medical device kits including AMS10833 Local Lower Extremity Pack I, AMS12947 In House Ocular Pack, AMS12947A In House Ocular Pack and AMS13043 Closure Kit. Produ

Al Amir Fresh Foods Issues Allergy Alert on Undeclared Sesame in Hummus Dip Products and Undeclared Milk in Tzatziki Cucumber Yogurt

FDA — Fri, 19 Jan 2024 11:00:00 EST

Al Amir Fresh Foods of Milwaukie, Oregon is recalling Al Amir brand hummus dip products due to undeclared sesame and Tzatziki Cucumber Yogurt due to undeclared milk.

Kilitch Healthcare India Limited Issues Amendments in Last Voluntary Nationwide Recall Press Release

FDA — Fri, 19 Jan 2024 00:00:00 EST

Mumbai, Maharashtra, Kilitch Healthcare India Limited is issuing an amendment in the last Nationwide press release dated November 13, 2023 issued for nationwide recall of various eye drops. There are corrections in product NDC No for the below mentioned products. These products were distributed nati

Hans Kissle Issues Allergy Alert on Undeclared Soy & Egg in "Hans Kissle Mexican Style Quinoa Salad"

FDA — Thu, 18 Jan 2024 00:00:00 EST

Hans Kissle of Haverhill, MA, is recalling its 7-ounce packages of MEXICAN STYLE QUINOA SALAD, deli salad, because the product contains undeclared egg and soy. People who have an allergy or severe sensitivity to egg and/or soy run the risk of serious or life-threatening allergic reaction if they con

Whitley’s Peanut Factory Issues an Allergy Alert on Undeclared Peanuts, Milk, Soy, Wheat, and Sesame for Limited Units of Deluxe Nut Mix 12oz (340g)

FDA — Thu, 18 Jan 2024 00:00:00 EST

Whitley’s Peanut Factory of Hayes, Virginia is recalling 12oz Deluxe Nut Mix with specific code dates because they may contain undeclared peanuts, milk, soy, wheat, and sesame. People who have an allergy or severe sensitivity to these ingredients run the risk of serious or life-threatening allergic

Brightfarms Recalls Spinach and Salad Kits Because of Possible Health Risk as a Result of Supplier Element Farms Recall

FDA — Wed, 17 Jan 2024 00:00:00 EST

BrightFarms has issued a voluntary recall of spinach grown by its supplier Element Farms in their Pompton Plains, New Jersey farm and distributed under the BrightFarms brand because the spinach has the potential to be contaminated with Listeria monocytogenes. Due to potential cross-contamination, Br

Big Island Candies Issues Allergen Alert on Undeclared Peanuts in “Makana Brownie Assortment”

FDA — Tue, 16 Jan 2024 00:00:00 EST

Big Island Candies of Hilo, Hawaii is voluntarily recalling 120 boxes of their Makana Brownie Assortment Box (batch 60) purchased from its Ala Moana Store located at 1450 Ala Moana Blvd., Honolulu, Hawaii between
December 13, 2023 – December 21, 2023 because the product contains undeclared peanuts.

World Green Nutrition, Inc. is Recalling ELV Alipotec Brand Mexican Tejocote Root Supplement Pieces (Raiz De Tejocote Mexicano Suplemento En Trozos), Net. Wt, 0.3 0Z (7g), Due to the Presence of Yellow Oleander in this Product

FDA — Fri, 12 Jan 2024 00:00:00 EST

WORLD GREEN NUTRITION, INC. is recalling ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g), due to the
presence of yellow oleander in this product. The consumption of yellow oleander can cause adverse effects on neurolog

Rizo Lopez Foods, Inc. Recalls Aged Cotija Mexican Grating Cheese (8oz) Because of Possible Health Risk

FDA — Thu, 11 Jan 2024 00:00:00 EST

Rizo Lopez Foods, Inc. of Modesto, CA is recalling a total of 344 cases of Aged Co􀆟ja Mexican Gratng Cheese (8oz), UPC 72724200043 batch number 4DW-23318 because it has the poten􀆟al to be contaminated with Listeria monocytogenes, an organism which can cause serious and some􀆟mes fatal infec􀆟ons

Update: Quaker Issues Revised Recall Notice with Additional Products Due to Possible Health Risk

FDA — Thu, 11 Jan 2024 00:00:00 EST

U.S. Trading Company of Hayward, CA is Recalling Dragonfly Jelly Bars Because it Contains Konjac Powder and May Present a Choking Hazard

FDA — Thu, 11 Jan 2024 00:00:00 EST

U.S. Trading Company of Hayward, CA is recalling Dragonfly jelly bars because it contains konjac powder and may present a choking hazard. Konjac and its consequent texture and consistency could pose a choking hazard to small children as well as adults with functional and/or anatomic abnormalities.