The Recall Desk

Hazard

Undeclared Ingredients recalls

127 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
127
Critical
55
Severe
19
Most recent
2026-09-02

Of the 127 undeclared ingredients recalls we have scored against our rubric, 55 (43%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 19 (15%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all undeclared ingredients recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

101–125 of 127

  • SevereFDA (Drugs)·D-1235-2014·2014-04-23

    Prolifta Dietary Supplement Recalled for Unapproved Erectile Dysfunction Ingredients

    Haute Health, LLC is recalling Prolifta dietary supplements because they may contain unapproved active ingredients used in erectile dysfunction drugs.

    Product
    Prolifta Dietary Supplement Prolifta, 400mg/capsule, Packaged in 1 and 2 capsule blister packs and 4, 12, and 24 capsule bottles Made in the USA Distributed by: Prolifta LLC 1+877.239.8231 www.proliftaherbal.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1220-2014·2014-04-16

    Dr. Ming's Chinese Capsule Recalled for Undeclared Sibutramine and Phenolphthalein

    Slim Beauty USA is recalling Dr. Ming's Chinese Capsule because it contains undeclared sibutramine and phenolphthalein, making it an unapproved new drug.

    Product
    Dr. Ming's Chinese Capsule (Ginger 50 mg, Camellia Sinensis 50 mg, Malus Domestica 50 mg, Propetary Blend 300 mg Cynara Scolymus, Hoodia, Siruline, Chitosan, 60-count bottles, Distributed by Natural Products, Doral, FL 33178.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1221-2014·2014-04-16

    Slim Beauty USA Recalls Magic Slim Capsules Containing Unapproved Ingredients

    Slim Beauty USA is recalling Magic Slim capsules nationwide because they contain undeclared sibutramine and phenolphthalein, making them unapproved new drugs.

    Product
    Magic Slim capsules (Ling Zhi, Ebony, Fox-nut, Tuckahoe, Seman Pruni, Dioscoreae, Wheat Germ, Nature Substance), 60-count bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-374-2014·2013-12-25

    Purity First Recalls Multi-Mineral Capsules for Undeclared Steroids

    Healthy Life Chemistry is recalling multi-mineral capsules because they contain undeclared steroid-like substances, making them unapproved new drugs.

    Product
    Multi-Mineral capsules, 200-count bottles, labeled in part as Healthy Life Chemistry, By Purity First, Manufactured for: Purity First Health Products, Inc. Healthy Life Chemistry 51 Florida Street, Farmingdale, NY 11735; 1-800-696-7017
    Category
    Drug
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-345-2014·2013-12-18

    Volcano Male Enhancement Capsules Recalled for Undeclared Pharmaceutical Ingredients

    Myson Corporation is recalling Volcano Male Enhancement capsules because they contain undeclared active pharmaceutical ingredients, making them unapproved new drugs.

    Product
    Volcano Male Enhancement 1500mg, 1-count capsule packaged in a black round plastic pop top container, (Proprietary Formula, Pueraria lobata, Cinnamon Bark, Cuscuta, Gui, Licorice, Altractylodes, Dang Condonopsis, Dismutase, Cornus, Rubus, Deng Sen Extract, Panax Ginseng, Cordycep
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-344-2014·2013-12-18

    Volcano Male Enhancement Liquid Recalled for Undeclared Pharmaceutical Ingredients

    Myson Corporation is recalling Volcano Male Enhancement Liquid because it contains undeclared active pharmaceutical ingredients, making it an unapproved new drug.

    Product
    Volcano Male Enhancement Liquid, 2 FL OZ (60 ml) bottle, www.volcanoenhancement.com, DISTRIBUTED BY VOLCANO Long Beach, CA 90813, UPC 6 09613 85996 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-021-2014·2013-12-04

    Jack Rabbit Herbal Supplement Recalled for Undeclared Prescription Ingredients

    Jack Rabbit, Inc. is recalling its J.R. Jack Rabbit All Natural Herbal Supplement because FDA testing found undeclared sildenafil and tadalafil.

    Product
    J.R. Jack Rabbit All Natural Herbal Supplement, One tablet can last 24-72 hours, 4-count tablets per blister pack, Order at: www.jackrabbitfourpack.com, Jack Rabbit Inc., 4355 Dow Road, Melbourne, FL 32934
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0222-2014·2013-11-27

    CTF Brand Tapioca Pearl Pandan Recalled for Missing Ingredient Labeling

    N A Trading Inc is recalling CTF Brand Tapioca Pearl Pandan because the packaging fails to list Artificial Color Yellow No. 5 and Brilliant Blue FD&C No. 1.

    Product
    CTF Brand Tapioca Pearl Pandan (Green Color), 14oz Plastic Bags, Packaged at 50 bags per case. Packaged in plastic heat-sealed pouch. Brand name is CTF with an illustration of a deer. Product labeling reads in part:"C.T.F. Brand TAPIOCA PEARL***EXPORTED: COMBINE THAI FOODS
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Drugs)·D-921-2013·2013-09-04

    Bethel 30 capsules recalled for undeclared active ingredients

    Bethel Nutritional Consulting, Inc. is recalling Bethel 30 capsules because FDA analysis found undeclared sibutramine and phenolphthalein, making the product an unapproved new drug.

    Product
    Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-837-2013·2013-08-14

    Reumofan Plus tablets recalled for undeclared active pharmaceutical ingredients

    Reumofan Plus tablets are being recalled because they were marketed without an approved NDA/ANDA and may contain undeclared active ingredients.

    Product
    Reumofan Plus, 30-count tablets per bottle, distriubted by Reumofan Plus USA, LLC and Reumofan USA, LLC, Springfield, PA, and manufactured by Riger Natural S.A., Mexico.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-828-2013·2013-08-07

    Green Planet Night Bullet Capsules Recalled for Unapproved Active Ingredients

    Green Planet Inc is recalling Night Bullet Capsules because they contain unapproved active ingredients for erectile dysfunction.

    Product
    Night Bullet Capsules, supplied in 1 count packets, produced by Green Planet Inc, Riverside, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-336-2013·2013-05-22

    FDA Recalls Mojo Nights Capsules for Unapproved Active Ingredients

    Performance Plus Marketing is recalling Mojo Nights Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.

    Product
    Mojo nights Capsules, Male Sexual Enhancer, supplied in 1 and 5 count blister packs, Distributed By: Mojo Health, Pompano Beach, FL I count blister UPC - 718122119738; 5 count blister UPC - 705105836430;
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-334-2013·2013-05-22

    FDA Recalls Blue Diamond Pill for Undeclared Sildenafil and Tadalafil

    Performance Plus Marketing, Inc. is recalling Blue Diamond Pill male sexual enhancement products because they may contain undeclared sildenafil, tadalafil, and analogues.

    Product
    BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH Distribution Los Angeles, CA 90026. 1 count blister: UPC 705105524764, 5 count blister: UPC 736211124012, 10 count blister: UPC 736211123916.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-328-2013·2013-05-22

    Evol Nutrition Recalls Mojo Nights for Her Due to Unapproved Ingredients

    Evol Nutrition is recalling Mojo Nights for Her capsules because they contain unapproved ingredients used to treat male erectile dysfunction.

    Product
    Mojo Nights for Her, 1 capsule, UPC 7 18122 12133 5, Distributed By: Mojo Health Lauderhill, FL 33351
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-335-2013·2013-05-22

    BLUE Diamond Platinum Capsules Recalled for Undeclared Active Ingredients

    Performance Plus Marketing is recalling BLUE Diamond Platinum Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.

    Product
    BLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By: DH Distribution Los Angeles, CA 90026 1 count blister UPC -608641933543; 5 count blister UPC - 608641932867; 10 count UPC -608641933536
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-338-2013·2013-05-22

    Casanova Capsules Recalled for Undeclared Sildenafil and Tadalafil

    Performance Plus Marketing is recalling Casanova Capsules because they may contain undeclared sildenafil and tadalafil, making them unapproved drugs.

    Product
    CASANOVA Capsules, 450 mg, MALE SEXUAL ENHANCER, supplied i n1 count blister packs, UPC 736211906892; Distributed by: Casanova Distributors, Tucker, GA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-327-2013·2013-05-22

    Evol Nutrition Recalls Mojo Nights Capsules for Unapproved Ingredients

    Evol Nutrition is recalling Mojo Nights capsules because they contain unapproved ingredients used to treat erectile dysfunction.

    Product
    Mojo Nights, 1 capsule, UPC 7 18122 11983 7, Distributed By: Mojo Health Lauderhill, FL 33351
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-332-2013·2013-05-22

    FDA Recalls Libigrow Capsules for Undeclared Active Ingredients

    Performance Plus Marketing, Inc. is recalling Libigrow capsules marketed without FDA approval. The product may contain undeclared sildenafil, tadalafil, and analogues.

    Product
    libigrow capsules, PERFORMANCE ENHANCER, supplied in 1, 5 and 10 count blister packs, Distributed By: H & K Nutraceuticals Los Angeles, CA 1 count blister: UPC 094922567611, 5 count blister: UPC 094922567628, 10 count blister: UPC 610585434253.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-337-2013·2013-05-22

    Mojo nights SUPREME Capsules Recalled for Undeclared Active Ingredients

    Performance Plus Marketing, Inc. is recalling Mojo nights SUPREME Capsules because the product was marketed without an approved NDA/ANDA and may contain undeclared sildenafil, tadalafil, and analogues.

    Product
    Mojo nights SUPREME Capsules, 1000 mg, Male Sexual Enhancer, supplied in 1 count blister packs, UPC 610585435915; Distributed By: Mojo Health, Pompano Beach, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-333-2013·2013-05-22

    FDA Recalls Unapproved Libigrow XXXTREME Capsules Containing Undeclared Ingredients

    The FDA is recalling Libigrow XXXTREME Capsules because they were marketed without approval and may contain undeclared sildenafil, tadalafil, and analogues.

    Product
    libigrow XXXTREME Capsules, MAXIMUM STRENGTH FORMULA, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By Kretek International, Inc. Moorpark, CA 930210 1 count blister: UPC 705105830735, 5 count blister: UPC 610585435939, 10 count blister: UPC 610585435922
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1326-2013·2013-04-24

    Siya Green Mukwhas Recalled for Unapproved and Undeclared Colors

    Miami Growers, Inc. is recalling Siya Green Mukwhas because the product contains unapproved and undeclared colors.

    Product
    Siya Green Mukwhas Net Wt. 200 gm (7 oz) Distributed by: Miami Growers, Inc. 80 Broadway, Jersey City, NJ 07306 Phone: 201-985-9322, Fax: 201-985-9569 Email: [email protected] Visit us: www.miamigrowersinc.com A Product of India
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-0936-2013·2013-02-06

    General Mills Recalls Betty Crocker Cake Mix for Undeclared Colors

    General Mills is recalling a limited quantity of Betty Crocker SuperMoist Golden Vanilla cake mix due to a labeling error involving undeclared FD&C color ingredients.

    Product
    Betty Croker, Super Moist Cake Mix, Golden Vanilla, NET WT 15.25 oz (432 g), UPC 0 16000 40993 4, Dist by General Mills Sales, Inc., Minneapolis, MN 55440. Case UPC code 1600040993000
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0742-2013·2012-12-12

    Blue Diamond Almond Breeze Almond Milk Recalled for Undeclared Cocoa

    HP Hood LLC is recalling Blue Diamond Almond Breeze Almond Milk because it may contain undeclared cocoa and evaporated cane juice.

    Product
    Blue Diamond Almond Breeze Almond milk Half Gallon (1.89 L) Paper Carton UPC: 4157005618
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-063-2013·2012-12-05

    Samantha Lynn Recalls Reumofan Plus Tablets for Undeclared Ingredients

    Samantha Lynn, Inc. is recalling Reumofan Plus Tablets because they contain undeclared drug ingredients, making them unapproved drugs.

    Product
    Reumofan Plus Tablets, 30-count bottle per Box, (remaining label information in Spanish)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0566-2013·2012-11-07

    Guava and Cheese Turnovers Recalled for Undeclared Allergens

    Productos El Gauchito is recalling Guava and Cheese Turnovers due to undeclared milk, wheat, soy, and food dyes.

    Product
    "***Productos El Gauchito Empanadillas Argentinas de Guayaba y Queso (Guava and Cheese Turnovers)***keep frozen or refrigerated***consumer contact: [email protected] Av. Minillas NM-16 Bayamon PR 00956***"
    Category
    Food
    Distribution
    1 state