Undeclared ingredient recalls

ORL Labs LLC is recalling ORL Organic Oral Care Cinnamint toothpaste, 4 oz. FDA sampling found progesterone, estradiol or dehydroepiandrosterone (DHEA) in the product, which the notice describes as cross-contamination. About 7,202 units were distributed nationwide in the USA.

Moderate·FDA·Nov 6, 2026·ORL Labs6 products

Nalpac Ltd. is recalling DTF Sexual Chocolates. The product contains sildenafil and tadalafil, which are not listed on the label. The product was sold to about 16 customers, some with multiple stores, and 253 boxes are affected.

Serious·FDA·Nov 4, 2026·DTF

Little Temptations Chocolatey Eyeballs (Hazelnut Praline) contain whey, a milk product, but were distributed in packaging that did not show milk on the label. The notice reports no injuries.

Moderate·FDA·Nov 3, 2026·Crystal Temptations

Primal Herbs Volume, sold as a herbal supplement, contains sildenafil—a prescription medication—that is not listed on the label. FDA testing confirmed the presence of this undeclared ingredient. The product was sold online between July 2 and September 19, 2025.

Serious·FDA·Oct 21, 2026·Primal Herbs

Evexias Health Solutions Amino Ultra capsules are mislabeled and do not declare fish oil as an ingredient. This poses a risk to people with fish allergies. The recall affects 30 bottles distributed across multiple states.

Moderate·FDA·Oct 21, 2026·Evexias Health Solutions

Walker Foods, Inc. recalled Marca El Pato Salsa para Enchiladas (28 oz cans) because the product contains salt, garlic, and onions that are not listed on the label. People with allergies or sensitivities to these ingredients could be at risk if they rely on the label to make safe choices.

Moderate·FDA·Oct 21, 2026·El Pato

Pur Aqua Sparkling Frost Cherry Limeade 17 oz. bottles may contain aspartame that is not listed on the label. The affected products have a best-if-used-by date of 032327 and were distributed in Florida. Aspartame is an artificial sweetener that must be clearly labeled for consumers who need to avoid it for health reasons.

Moderate·FDA·Oct 21, 2026·Pur Aqua

Holsum Spinach Flour Tortillas (large, 8-count packages) contain FD&C Blue No. 1 and FD&C Yellow No. 5 food dyes that are not listed on the label. People with sensitivities or allergies to these dyes may be affected. The affected product was distributed in Puerto Rico and the US Virgin Islands.

Moderate·FDA·Oct 21, 2026·Holsum

El Ruisenor De Mexico, Inc. is recalling Fritura mixed dry fruit because the product contains wheat, Yellow #5, and Yellow #6 that are not declared on the label. The product was sold in 1 lb, 5 lb, and 25 lb clear plastic packages. People with wheat allergies or sensitivities to these food dyes could have a serious reaction if they consume this product.

Moderate·FDA·Oct 20, 2026·El Ruisenor De Mexico61 products

WAP Sensual Enhancement Capsules were sold without FDA approval and contain three undeclared prescription medications: sildenafil, tadalafil, and flibanserin. These are potent drugs that require a doctor's prescription and can cause serious health problems, especially in people taking other medications or with certain medical conditions.

Serious·FDA·Oct 20, 2026·Erotic Enhancers

PepsiCo is recalling specific 28 oz. bottles of Gatorade Lemon Lime, Lemon Lime Zero, Orange, and Orange Zero because they contain Yellow No. 5 and/or Yellow No. 6 food dyes that are not listed on the label. This is a concern for people with allergies or sensitivities to these dyes, or those who avoid them for dietary reasons.

Moderate·FDA·Oct 14, 2026·Gatorade

Some 12-ounce cans labeled as 7Up Tropical Zero Sugar actually contain full-sugar soda instead. This affects consumers who chose the zero-sugar version, particularly those managing sugar intake for health reasons like diabetes. The affected cans were distributed in Utah with a best-by date of March 17, 2027.

Moderate·FDA·Oct 7, 2026·7UP

Khazana Spice Magic Fennel Candy contains Yellow 5, Yellow 6, Red 3, and Blue 1 food dyes that were not declared on the label. These dyes can trigger allergic reactions or other health issues in people with sensitivities or those who avoid certain additives for medical or religious reasons.

Moderate·FDA·Oct 7, 2026·Khazana

FDA testing found that one lot of Babies' Magic Tea Baby Sleep Gripe Water contains ethanol, methanol, and isopropanol that are not listed on the label. These alcohols can impair the central nervous system, especially in infants, and may cause drowsiness, nausea, vomiting, or more serious effects depending on how much is used.

Serious·FDA·Oct 6, 2026·Pacific Health Sciences

Macleods Pharmaceuticals has recalled Olanzapine Tablets USP 5 mg (lot BOB22321A, expiring 07-31-2027) because testing found organic impurities above acceptable limits. The affected bottles were distributed nationwide. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·MacLeods Pharma

Elegant Foods' 9-inch Carrot Cake contains Yellow #5 and Yellow #6 food coloring in the carrot decoration, but these ingredients are not listed on the product label. This poses a risk to people with dye sensitivities or allergies who rely on label information to make safe food choices.

Moderate·FDA·Sep 23, 2026·Elegant Foods3 products

Wonton Specialist Inc. is recalling six products sold as pan fried noodles, wonton noodles, lo mein noodles, cooked noodles, wonton skins and dumpling skins. The products contain FD&C Red No. 40, a synthetic food dye, but the dye is not listed on the label. The products were distributed in New York, New Jersey and Pennsylvania, and no injuries have been reported.

FDA·Sep 9, 2026·Wonton Specialist6 products

SUPPLX.com's Business Pill and Branch Manager for Men dietary supplements contain yohimbine that is not listed on the labels. FDA testing found dangerously high levels of this substance, which can cause serious heart problems, severe high blood pressure, and other dangerous side effects—especially in people taking stimulants or certain medications.

Serious·FDA·Sep 3, 2026·Supplx.com

Hikma Pharmaceuticals is recalling specific lots of Ramipril Capsules 10 mg because testing found higher-than-allowed levels of dicyclohexylurea, a process impurity. The affected lots are AC5470A and AC5470B, both expiring July 2027. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Hikma Pharmaceuticals

Lipofit Extreme Fat Burner 2.0 (Lot 25M12F, expiration 09/2027) contains undeclared fluoxetine, a prescription antidepressant, in the daytime tablets and undeclared 2,4-dinitrophenol (DNP), a toxic pesticide, in the nighttime tablets. Neither ingredient is approved for use in dietary supplements, and DNP is not approved by the FDA for any use in humans.

Serious·FDA·Aug 27, 2026·Lipofit

Honeyville Yellow Color 1 Gallon contains undeclared Red #40 food dye, which is not listed on the label. The product was distributed to food manufacturers in Nevada, Arizona, Oregon, and California. People with allergies or sensitivities to Red #40 could have an adverse reaction if exposed without knowing the ingredient is present.

Moderate·FDA·Aug 19, 2026·Honeyville

Buy-Herbal's Kian Pee Wan Capsules contain two prescription drug ingredients—dexamethasone and cyproheptadine—that are not listed on the label and were not approved by the FDA. The product was sold online through eBay. No injuries have been reported.

Serious·FDA·Aug 19, 2026·Buy-Herbal

Asian America Trading recalled approximately 996 pounds of ready-to-eat fish skin crackers (sold under brands including UN CHI and others) because they were produced in China, a country not permitted to export this type of product to the United States. The products were discovered during routine inspections. No illnesses have been reported.

Serious·USDA·Aug 17, 2026·UN CHI

Eunha Fisheries Co., LTD frozen flounder sashimi with sauce contains undeclared allergens: wheat, soy, sesame, Yellow #5, and Blue #1. The product label does not warn consumers about these ingredients. People with allergies to these substances could have a serious reaction if they consume this product.

Moderate·FDA·Aug 12, 2026·Eunha Fisheries2 products

Man Fon is recalling two wonton wrapper products: Man Fon Extra Thin Won Ton Wrappers in 10 oz packages, and wonton wrappers sold in clear plastic bags, including 16 oz bags and 4-lb bags labeled "Wonton Noodles." The products contain Yellow #5 and Yellow #6 food dyes that are not listed on the label. The product went mainly to California restaurants, with some sent to New Mexico grocery stores.

Moderate·FDA·Jul 29, 2026·Man Fon2 products

Joywin is recalling three imitation crab products sold under the Island Pacific and Nautilus brands: Island Pacific imitation crab sticks, Island Pacific imitation crab flakes, and Nautilus imitation crab sticks. The packages do not list sodium tripolyphosphate (STTP) on the label. The products were distributed in California. No illnesses or injuries have been reported.

FDA·Jul 29, 2026·Island Pacific3 products

D'Dioses Fruit Pops ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 dyes. These allergens are not listed on the label and could pose a serious risk to people with allergies or sensitivities. The product was distributed in New Jersey, Connecticut, New York, and Pennsylvania.

Serious·FDA·Jul 22, 2026·D'Dioses Fruit Pops16 products

Four lots of Unique Pharmaceutical Cetirizine Hydrochloride 5 mg tablets were found to be cross-contaminated with ranitidine. The contamination was discovered when pharmacy staff noticed red discoloration on some tablets. People with sensitivity to ranitidine could experience serious allergic reactions.

Serious·FDA·Jul 18, 2026·Unique Pharmaceutical Laboratories

Wise Foods Onion Rings (3.75 oz bags) contain undeclared Yellow 5, Yellow 6, Blue 1, and unapproved Red 3 food dyes. The product was distributed in seven states. No injuries have been reported.

Moderate·FDA·Jul 15, 2026·Wise

PH Labs is recalling two dietary supplements, Ocular Plus and Vista MAX, because they contain Yellow No. 5 dye that is not listed on the label. Ocular Plus was distributed by L.A. Farmacia Natural and Vista MAX by Vision of Health, with about 6,967 units of each affected. The products went to two local retail stores, and no injuries have been reported.

Moderate·FDA·Jul 8, 2026·PH Labs2 products