FDA food recalls

Riverence Provisions LLC is recalling Smoked Trout Dip because the label does not declare milk, even though the product contains cream cheese and sour cream. People with milk allergies could have a serious reaction if they eat this product. The recall affects specific lot numbers distributed across several states.

F&S Fresh Foods ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich contains sesame that is not listed on the label. The sandwich has visible sesame seeds, but the package only declares egg, milk, soy, and wheat as allergens. This poses a serious risk to people with sesame allergies.

Mei Yu Cheng Da Trading olive skewers contain cyclamates, a sweetener banned for use in food in the United States. The product was distributed in New York, Pennsylvania, and Florida. No injuries have been reported so far.

Dadi Nongfu brand dried salt chili vegetables contain cyclamates, a sweetener banned for food use in the United States. The product was distributed in New York, Pennsylvania, and Florida. No injuries have been reported.

Connecticut Crab Company LLC is recalling crab cakes produced on March 9, 11, 13, 16, and 18, 2026, that may have been stored at unsafe temperatures. This could allow dangerous bacteria called Clostridium botulinum to grow. The affected crab cakes were sold to food service businesses in New York and New Jersey.

Red Bull Extreme Male Enhancement Supplement pouches contain sildenafil, a prescription drug ingredient that was not listed on the label. Sildenafil can cause serious health problems, especially if you take other medications or have certain medical conditions. The affected product was distributed in New Jersey with batch number ORB524 and a May 2024 manufacturing date.

Blue Bull Extreme Male Enhancement Supplement contains undeclared sildenafil, a prescription medication. The product was not labeled to indicate the presence of this drug. Sildenafil can cause serious health effects, especially if you take other medications or have certain medical conditions.

Pure Vitamins and Natural Supplements, LLC is recalling Boner Bears Honey Male Enhancement pouches because they contain hidden prescription medications—sildenafil and tadalafil—that are not listed on the label. These drugs can cause serious health problems, especially for people taking certain other medications or with heart conditions.

Zarlengo's Double Dark Chocolate Gelato contains soy lecithin but the label does not list soy as an allergen. This poses a serious risk to people with soy allergies who rely on label information to avoid allergens. The recall affects 1-gallon containers with specific lot codes sold in Illinois, Indiana, and Texas.

Zarlengo's Chocolate Gelato contains soy lecithin but does not clearly list soy as an allergen on the label. This poses a serious risk to people with soy allergies. The recall affects 6 fl oz cups, 16 fl oz cups, 32 fl oz cups, and 1-gallon buckets distributed in Illinois, Indiana, and Texas.

Zarlengo's Chocolate Chocolate Chip Gelato contains soy lecithin but does not label soy as an allergen on the package. This poses a risk to people with soy allergies. The recall affects multiple package sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon and 2-gallon buckets) sold in Illinois, Indiana, and Texas.

Imu-Tek Colostrum-5 Powder (Lot #22, expiration 020528) may not have been processed adequately, which could allow harmful bacteria to survive. The affected product was distributed across 29 states. No illnesses have been reported so far.

Imu-Tek Animal Health is recalling Colostrum-5 120-capsule bottles (Lot #013, expiration 092826) because the product may be under-processed, which can affect its safety. The affected bottles were distributed across 33 states.

HEYTEA USA's Coconut Drink 1 (1L cartons) contains milk that is not listed on the label. The product was distributed to food service establishments in multiple states. This poses a serious risk to anyone with a milk allergy or severe intolerance.

Undeclared milk.

Mama Rose's Prickly Pear Salad Dressing in 12 oz glass bottles contains sulfites that are not listed on the label. Sulfites can cause serious allergic reactions in people with sulfite sensitivity. The affected bottles were distributed in Arizona with sell-by dates of June 9 or June 25, 2026.

Mei Heong Yuen Garlic Flavor Roasted Peanuts (9.17 oz) contain cyclamates, a sweetener banned in the United States. The product was distributed to multiple states under UPC 6912449124329 with manufacture date July 10, 2025. No injuries have been reported.

Mei Heong Yuen walnut-flavor roasted peanuts contain sodium cyclamate, a sweetener banned in the United States. The 9.17 oz packages were distributed to multiple states. No illnesses have been reported.

Mei Heong Yuen tangerine flavor roasted peanuts contain sodium cyclamate, a sweetener banned in the United States. The product was distributed to 19 states. No injuries have been reported.

Lone Star Dairy Products LLC is recalling spray dried milk powder products because Salmonella bacteria was found during testing of finished products. The recall affects specific lot codes of NFDM Low Heat, NFDM High Heat, and SMP Medium Heat products sold in 25 kg bags and 1 metric ton totes.

JFE Franchising is recalling certain vegetable dumpling products because they may contain small pieces of glass. The recall includes Dumpling Party Tray (20-piece and 40-piece packages) and Cheetos Flamin' Hot Loaded Dumpling Vegetable products sold across the United States.

JFE Franchising Inc. is recalling Dumpling Vegetable products (4.5 oz and 5.7 oz packages) because they may contain glass fragments. The recall affects products distributed across the United States. No injuries have been reported.

Divided Sunset Multi Collagen Peptides (8 oz pouch) contain egg and fish ingredients but do not clearly label them as allergens on the package. The ingredient list mentions eggshell membrane collagen and marine collagen but fails to state "EGG" or identify the fish species as required by law. This poses a risk to people with egg or fish allergies.

Pocas International Corp. is recalling Popping Boba RTD Mango Passion Fruit Green Tea because of a packaging integrity issue that may allow the product to degrade or become contaminated. The recall affects 517 cases distributed across nine states and Canada. No injuries have been reported.

Pocas International Corp. is recalling its Popping Boba RTD Strawberry Dragon Fruit/Oolong Tea because the packaging may not be properly sealed. This could allow the product to spoil or become contaminated. The affected product was distributed to nine states and Canada.

Pocas International Corp. is recalling Popping Boba RTD Mixed Berry Hibiscus Tea because of a packaging integrity issue that may allow the product to spoil or become contaminated. The recall affects 148 cases distributed to New York, Virginia, Florida, Massachusetts, Texas, Louisiana, Utah, California, and Canada.

Pocas International Corp. is recalling its Popping Boba RTD Peach Oolong Tea (12-pack, 13.8 oz bottles) due to a packaging integrity issue that could compromise product quality. The affected product was distributed to nine states and Canada. No injuries have been reported.

Distribuidora de Alimentos Sendero's Doraditas de Azucar cookies are missing allergen warnings on the label for wheat and soy. If you have an allergy to either ingredient, consuming this product could cause a serious reaction. About 500 units were distributed in Texas.

Distribuidora de Alimentos Sendero LLC is recalling Gorditas de Azucar and Doraditas products (UPC 860010238134) because the packaging does not list wheat and soy as ingredients, even though they are present in the product. This poses a serious risk to people with wheat or soy allergies. The recall affects 2,500 units distributed in Texas with all expiration dates.

SiluetaYa Mexican Tejocote Roots Supplement Pieces contain yellow oleander, a toxic plant that can cause serious illness. The affected product was sold online in Arizona, California, New Mexico, New York, Texas, and Utah. This is a Class I recall, the FDA's most serious category.