Recent FDA food recalls

29,505 FDA food recall reports, newest first, from openFDA's data updated 2026-10-23. 2,331 name a barcode of a product we list, and link to it.

A recall applies to the lots and codes it lists, not every package of a product. “Class” is FDA's rating of how serious the risk is.

• 2013-10-02 · Class II · Closed by FDA Snoqualmie Falls Candy Factory, LLC: Coconut Brittle's is labeled in parts: "***COCONUT BRITTLE***INGREDIENTS: Coconut (preserved with metabisulfate), white sugar, glucose, butter (cream, salt)… Reason: Finished product labels declared butter or cream but milk is not listed. Recall F-1953-2013 details
• 2013-10-02 · Class II · Closed by FDA Snoqualmie Falls Candy Factory, LLC: Coconut Peanut Brittle's label is read in parts:"***COCONUT PEANUT BRITTLE***INGREDIENTS: Coconut (preserved with sodium metabisulfate), peanuts, white sugar… Reason: Finished product labels declared butter or cream but milk is not listed. Recall F-1952-2013 details
• 2013-10-02 · Class II · Closed by FDA Snoqualmie Falls Candy Factory, LLC: Almond Brittle's label is read in parts:"***ALMOND BRITTLE***INGREDIENTS: Sugar, corn syrup, almonds, brown sugar, butter (cream, salt), baking soda, salt. NO… Reason: Finished product labels declared butter or cream but milk is not listed. Recall F-1951-2013 details
• 2013-10-02 · Class II · Closed by FDA Snoqualmie Falls Candy Factory, LLC: Pecan Brittle's label is read in parts: "***PECAN BRITTLE***INGREDIENTS: Sugar, corn syrup, pecans, brown sugar, butter (cream, salt), baking soda, salt. NO… Reason: Finished product labels declared butter or cream but milk is not listed. Recall F-1950-2013 details
• 2013-10-02 · Class II · Closed by FDA Mothers Milk Bank: Human breast milk, pasteurized, 4 oz, in bottles; Pasteurized Human Milk,Hospital Grade Milk. Mother's Milk Bank 751 S. Bascom Abe.San Jose, CA 95128 Reason: Human Breast milk was collected from a donor that tested reactive for Hepatitis B in a screening test. Recall F-1949-2013 details
• 2013-10-02 · Class II · Closed by FDA Semifreddi's Inc.: Chocolate Dipped Almond Biscotti, in various sizes, wrapped in plastic, with "Enjoy By" dates prior to 091614, manufactured by Semifreddi's Inc, Alameda, CA… Reason: Semifreddi's Almond Biscotti and Semifreddi's Chocolate Dipped Almond Biscotti are being recalled due to undeclared allergens, milk and soy; butter did not list milk as a subingredient; lecithin did not list soy as a… Recall F-1948-2013 details
• 2013-10-02 · Class II · Closed by FDA Semifreddi's Inc.: Almond Biscotti, 1 oz. and 0.5 oz. wrapped in plastic, with "Enjoy By dates prior to 091614, manufactured by Semifreddi's Inc, Alameda, CA. Product size and… Reason: Semifreddi's Almond Biscotti and Semifreddi's Chocolate Dipped Almond Biscotti are being recalled due to undeclared allergens, milk and soy; butter did not list milk as a subingredient; lecithin did not list soy as a… Recall F-1947-2013 details
• 2013-10-02 · Class I · Closed by FDA Irene's Bakery & Gourmet Kitchen, Inc.: Irene's Black & White Cookies, 8 oz. (226.4g) All Natural. Ingredients: Sugar, wheat flour, water, eggs, canola oil, unmodified food starch, corn syrup… Reason: Undeclared whey powder (milk allergen) sub-ingredient of chocolate confectionery coating used in manufacturing of Black & White Cookies. Recall F-1946-2013 details
• 2013-10-02 · Class II · Closed by FDA Restaurant Depot: JAMES FARM brand CUT GREEN BEANS (EJOTES CORTADOS), FRESH FROZEN, NET WT. 32 OZ. (2 LBS.) 907 g, UPC 7 60695 01004 2, PRODUCT OF POLAND -- Distributed by… Reason: The product was found to be contaminated with Listeria monocytogenes based on private laboratory testing. Recall F-1945-2013 details
• 2013-10-02 · Class II · Closed by FDA American Nut Company: Fancy Mixed Nuts (25lbs), Mixed Nuts (25lbs), and Super King Fancy Mixed Nuts (25lbs) Reason: American Nuts is recalling Mixed Nuts because they may contain undeclared wheat allergen. Recall F-1944-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1943-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 100 capsules***Manufactured for:HealthMax… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1942-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 150 tablets***Manufactured for:HealthMax Products… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1941-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:"MAX CoQ-10 80 mg***DIETARY SUPPLEMENT 300 Capsules***6 65176 25166… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1940-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: MAX Brand SOY ISOFLAVONES, 90 Count Capsules; MAX Brand ULTRA… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1939-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1938-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIETARY SUPPLEMENT 300 Capsules***0 65176… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1937-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:"MAX Organic OPC31 Grapeseed Extract***NEW WITH… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1936-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:"MAX Organic Blueberry***Dietary Supplement 100 CAPSULES***6 65176 62165… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1935-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1934-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1933-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10***Dietary Supplement 200 Capsules***6 65176 32608… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1932-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 7***HealthMax Products… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1931-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10***DIETARY SUPPLEMENT 90 Capsules***6 65176 30162 9***Manufactured in FDA… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1930-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(30ml)***". Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1929-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1928-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Supplement 100 Softgels***6 65176 01115 3***Manufactured… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1927-2013 details
• 2013-10-02 · Class II · Closed by FDA Healthmaxx Global Inc.: Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hyper II DHA/EPA Refined Deep Sea Fish Oil 50% DHA - 30% EPA***Dietary Supplement 100… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1926-2013 details
• 2013-10-02 · Class II · Closed by FDA Healthmaxx Global Inc.: MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:"MAX Bio-Cell CollagenII Dietary Supplement 100 Softgels*** 0 65176 08108… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1925-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX***BRAZILIAN BEE PROPOLIS DIETARY SUPPLEMENT 180 Softgels***6 65176… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1924-2013 details
• 2013-10-02 · Class I · Closed by FDA Healthmaxx Global Inc.: MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:"MAX SUPER SELENIUM 250 ***Dietary Supplement 180 Tablet***0 65176 06756… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1923-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***Manufactured in FDA… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1922-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG 200 Count… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1921-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Glucosamine 1500mg***200 Tablets***6 65176 60566… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1919-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1918-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1917-2013 details
• 2013-10-02 · Class III · Closed by FDA Healthmaxx Global Inc.: Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 Count Tablets. Product labeling reads… Reason: In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained… Recall F-1916-2013 details
• 2013-10-02 · Class III · Closed by FDA Shenandoah Growers, Inc.: Basil, fresh, Giant brand, packaged in 2.5 oz. package and labeled in part ***Distributed by FoodHold USA Landover, MD 20785*** Reason: Fresh basil may be adulterated with pesticides. Recall F-1915-2013 details
• 2013-10-02 · Class III · Closed by FDA Shenandoah Growers, Inc.: Fresh Herbs Everyday Basil, Shenandoah Growers brand, packaged in .75 oz; 2 oz.; and 2.5 oz. in 3 count and 6 count cardboard sleeves and labeled in part… Reason: Fresh basil may be adulterated with pesticides. Recall F-1914-2013 details
• 2013-10-02 · Class II · Closed by FDA Gourmet Express Marketing, Inc.: Breaded, frozen shrimp packaged in plastic bags labeled in part: BREADED SHRIMP; NET WEIGHT; 2.0 LBS or 3 LBS Reason: Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat allergens. Recall F-1913-2013 details
• 2013-10-02 · Class II · Closed by FDA Maplehurst Bakeries, Inc.: Meijer 8 Inch Carrot Uniced Split Cake Layers (product is packed in bulk cartons of 24 units/paper bags lined with flexible blue plastic liner). Reason: Product was found to contain foreign material, flexible plastic. Recall F-1912-2013 details
• 2013-10-02 · Class I · Closed by FDA Garden-Fresh Foods, Inc.: spartan fresh selections american potato salad, Net Wt. 16 oz (1 LB) 454g. UPC 11213-90320. Reason: One lot of Spartan Fresh Selections American Potato Salad has the potential to be contaminated with Listeria monocytogenes. Recall F-1911-2013 details
• 2013-10-02 · Class I · Closed by FDA KDK Management, Inc., dba Bubbles Baking Co.: First Street Blueberry Muffins Loaf (S 45383), 16 oz., 12 trays/case, UPC 0 41512 10854 9. Reason: Bubbles Baking Co. is recalling Blueberry muffins and Loaf cakes because they may contain undeclared milk and soy. Products we list: First Street Blueberry Sliced Loaf Cake, Blueberry Recall F-1910-2013 details
• 2013-10-02 · Class I · Closed by FDA KDK Management, Inc., dba Bubbles Baking Co.: First Street Blueberry Muffins (S 45395), 14 oz., 9 trays/case, UPC 0 4151210833 4 Reason: Bubbles Baking Co. is recalling Blueberry muffins and Loaf cakes because they may contain undeclared milk and soy. Products we list: First Street Blueberry Muffins, Blueberry Recall F-1909-2013 details
• 2013-09-25 · Class I · Closed by FDA Tampa Maid Foods, Inc.: Frozen, 4/3 lb unlabeled bags contained in a master carton box labeled in part: "Portico Brand 4/3 lb 170585 Breaded Scallops***Net Wt 12 lb (5.44… Reason: Incorrect Ingredient Labeling Recall F-1908-2013 details
• 2013-09-25 · Class III · Closed by FDA Novartis Consumer Health: Benefibre, Orange Creme Chewables, 36ct and 100ct chewable tablet bottles. Foreign labeling: Novartis Consumer Health Canada Inc, Mississauga, ON. Reason: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging. Recall F-1907-2013 details
• 2013-09-25 · Class III · Closed by FDA Novartis Consumer Health: Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippany, NJ. Reason: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging. Recall F-1906-2013 details
• 2013-09-25 · Class III · Closed by FDA Novartis Consumer Health: Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ. Reason: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging. Recall F-1905-2013 details
• 2013-09-25 · Class III · Closed by FDA Novartis Consumer Health: Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet bottles. Novartis Consumer Health, Inc, Parsippany, NJ. Reason: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging. Recall F-1904-2013 details
• 2013-09-25 · Class III · Closed by FDA Novartis Consumer Health: Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis Consumer Health, Inc, Parsippany, NJ. Reason: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging. Recall F-1903-2013 details

Source: openFDA food enforcement reports (CC0).