Undeclared ingredient recalls

Galaxy RG Corp's Cake de Fresa y Chocolate (48 oz) contains undeclared food coloring—Yellow #5, Yellow #6, and/or Red #40—which are not listed on the label. People with allergies or sensitivities to these dyes may be at risk if they consume the product. The affected cakes were distributed in Florida and Texas with expiration dates between April 3 and May 3, 2026.

Galaxy RG Corp's Cake de Coco Coconut Cake (47 oz) contains undeclared food dyes: Yellow #5, Yellow #6, and/or Red #40. These dyes are not listed on the package label. The recall affects specific lot codes with expiration dates between April 3 and May 3, 2026, distributed in Florida and Texas.

Galaxy RG Corp's Cake de Capuchino contains food dyes (Yellow #5, Yellow #6, and/or Red #40) that are not listed on the package label. People with allergies or sensitivities to these dyes could have a reaction if they consume the product without knowing the dyes are present.

Galaxy RG Corp's Capuchino Syrup Cone Cake (13 oz) contains undeclared food colorings: Yellow #5, Yellow #6, and/or Red #40. These dyes are not listed on the package label. The affected product was distributed in Florida and Texas with expiration dates between April 3, 2026 and May 3, 2026.

Galaxy RG Corp's Rollitos de DulceLeche Caramel Rolls (15 oz) contain Yellow #5, Yellow #6, and/or Red #40 food colorings that are not listed on the package label. This matters because people with sensitivities or allergies to these dyes, or those who avoid them for other reasons, need to know they are present. The recall affects specific lot numbers sold in Florida and Texas with expiration dates between April 3 and May 3, 2026.

Galaxy RG Corp's Rollitos de Guava (Guava Rolls) 15 oz packages contain undeclared food color additives—Yellow #5, Yellow #6, and/or Red #40—that are not listed on the label. People with sensitivities or allergies to these dyes may have an allergic reaction if they consume the product.

Galaxy RG Corp's Jumbo Neapolitan ice cream (26 oz) contains Yellow #5, Yellow #6, and/or Red #40 food dyes that are not listed on the package label. These dyes can cause allergic reactions in people with sensitivities to artificial colors. The affected product was distributed in Florida and Texas with expiration dates between April 3 and May 3, 2026.

Galaxy RG Corp's Napolitano Neapolitan ice cream (22 oz) contains undeclared food colors: Yellow #5, Yellow #6, and/or Red #40. These dyes are not listed on the package label. The affected products were distributed in Florida and Texas with expiration dates between April 3 and May 3, 2026.

Galaxy RG Corp's Jumbo Brazo Gitano Caramel Roll (40 oz) contains Yellow #5, Yellow #6, and/or Red #40 food dyes that are not listed on the label. These dyes can trigger allergic reactions or sensitivities in people who avoid them for medical or dietary reasons. The affected products were distributed in Florida and Texas with expiration dates between April 3 and May 3, 2026.

Galaxy RG Corp's Brazo Gitano Caramel Sweet Rolls (24 oz) contain undeclared food colorings: Yellow #5, Yellow #6, and/or Red #40. The affected products have expiration dates from April 3 to May 3, 2026, and were distributed in Florida and Texas. Consumers with allergies or sensitivities to these dyes may be at risk.

Refresqueria Estrella Inc. is recalling Bebida de Parcha (passion fruit drink) in multiple sizes because the product contains FD&C Red 40 food coloring that was not declared on the label. This affects bottles sold in Puerto Rico with specific production lot codes and expiration dates from March through May.

Amneal Pharmaceuticals is recalling Primidone 50 mg tablets (NDC 53746-544-01, lot AM251676) due to potential cross-contamination with Acemetacin during manufacturing at the API supplier. The contamination could affect the safety or effectiveness of the medication.

Amerisource Health Services has recalled certain batches of Primidone Tablets, USP, 50 mg due to cross-contamination during manufacturing. The tablets contain trace amounts of Acemetacin, a different active pharmaceutical ingredient, which should not be present in this medication.

Primidone tablets distributed by American Health Packaging were found to contain trace amounts of Acemetacin, a different active pharmaceutical ingredient, due to cross-contamination during manufacturing. The affected lot (1027583, expiring 09/30/2027) contains approximately 63,500 tablets distributed nationwide. No injuries have been reported.

Golden State Medical Supply's Primidone Tablets (250 mg) contain trace amounts of Acemetacin, a different medication, due to cross-contamination during manufacturing. This affects two lots distributed nationwide. No injuries have been reported.

Lannett Company's Primidone Tablets 250mg were contaminated during manufacturing with trace amounts of Acemetacin, a different active pharmaceutical ingredient. The contamination affected specific lot numbers distributed nationwide. No injuries have been reported.

JXK Enterprises is recalling Boner Bears Chocolate (Lot #BB21125) because FDA testing found sildenafil, the active ingredient in prescription Viagra, in the product—but it was not listed on the label. Sildenafil can cause serious interactions with certain heart and blood pressure medications and poses health risks for people with diabetes, high blood pressure, or heart disease.

Swad Mango Flavored Masala Candy contains Blue 1 food dye that is not listed on the label. Blue 1 is an FDA-approved color additive, but it must be clearly declared on the package. People with sensitivity or allergy to this dye would not know it is present.

XD Investments LLC recalled Better Weather Fix Elixir dietary supplements after FDA testing found they contain undeclared mitragynine and mitragynine pseudoindoxyl—potent kratom alkaloids not listed on the label. These substances can cause serious health effects including rapid heart rate, hallucinations, severe addiction, and in rare cases, fatal respiratory depression, especially when combined with other medications or drugs.

Bee Well Honey Farm & Supply Inc. is recalling Raw & Unfiltered Wildflower Honey in 12 oz, 22 oz, and 44 oz sizes after FDA testing found high levels of C4 sugar, which indicates possible adulteration or blending with non-honey sweeteners. The product was distributed to retailers in South Carolina.

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.

Nalpac is recalling DTF Sexual Chocolate because it contains sildenafil and tadalafil—prescription drug ingredients found in Viagra and Cialis—that were not listed on the label. These hidden ingredients can dangerously lower blood pressure, especially if you take nitrate medications like nitroglycerin.

Kian Pee Wan capsules, sold online as a dietary supplement for weight gain and appetite, contain two hidden prescription drugs: dexamethasone (a corticosteroid) and cyproheptadine (an antihistamine). These drugs were not listed on the label. Taking these undeclared drugs can cause serious health problems including infections, high blood sugar, psychiatric issues, and withdrawal symptoms if stopped abruptly.

Lowes Foods sour cream and onion flavored potato chips (8 oz bags) have incorrect Nutrition Facts labels. The sodium content is listed lower than it actually is, and monosodium glutamate (MSG) is not listed as an ingredient even though it is present in the product. This matters if you avoid high sodium or MSG for health reasons.

Bader Enterprises Premium Food Bubble Gum contains undeclared food coloring (FD&C Blue 1 Lake and FD&C Blue 2 Lake) that is not listed on the package label. This poses a risk to people with allergies or sensitivities to these dyes. The affected product was sold in 2.5 oz packages with a best-by date of December 2028.

MR. 7 SUPER 700000 capsules contain hidden prescription drugs—sildenafil and tadalafil—that are not listed on the label. These are serious medications that can interact with other drugs and cause health problems. The product was sold without FDA approval.

Mojo Max Fusion XXX capsules contain hidden prescription drugs—sildenafil and tadalafil—that were not listed on the label. These are potent medications that can cause serious health problems, especially if you take other drugs or have certain heart or blood pressure conditions. The FDA has not approved this product for sale.

SILINTAN 25 pills, sold in 25-count bottles, contain an undeclared ingredient called meloxicam, a prescription pain reliever. The FDA found this ingredient was not listed on the label and the product was not approved by the FDA. The recall affects all lots currently in use.

Agebox iKids-Growth Night Formula contains ibutamoren, a substance not listed on the label or approved by the FDA for this product. The affected 60-count bottles were sold online through Agebox.com and Amazon.com. No injuries have been reported.

Agebox iKids-Growth Day Formula capsules contain an undeclared drug ingredient called ibutamoren that was not approved by the FDA. The product was sold without proper FDA authorization. This affects 60-count bottles with lot numbers 23101201, 24080801, and 25020701.