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.

26–50 of 127

  • CriticalFDA (Drugs)·D-1009-2019·2019-03-20

    Golean DETOX capsules recalled for undeclared sibutramine and phenolphthalein

    Golean Detox US is recalling Golean DETOX capsules because FDA analysis found undeclared sibutramine and phenolphthalein, ingredients not approved for marketing in the US.

    Product
    Golean DETOX capsules, 14 Net: 56 g, 14 packets containing 2 capsules per packet, 28-count capsules per box, MAT XI S.G Co., LTD, Head office: J29 Vo Thi Sau Street, Thong Nhat Ward, Bien Hoa City, Dong Nai Province, Viet Nam; Manufactory: 148/9 Tan Tien Ward, Bien Hoa City, Dong
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·117-2018·2018-11-23

    Chunwei Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens

    Chunwei, Inc. is recalling meat and poultry products because they are misbranded and may contain undeclared allergens and MSG, with no confirmed illness reports.

    Product
    Chunwei, Inc. Recalls Meat and Poultry Products Due to Misbranding and Undeclared Allergens and Monosodium Glutamate
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0007-2019·2018-10-10

    Baker's Service Recalls Guava Pastry for Undeclared Wheat and Color Additives

    Baker's Service of South Florida is recalling 975 cases of Guava Pastry because the labeling failed to declare wheat and specific color additives.

    Product
    Guava Pastry. The product is packed in a cardboard box. The firm marks the Guava Pastry option printed on the box. Labeling for the cardboard box reads in part: WHOLESALE FROZEN BAKERY PRODUCTS, TRACY BAKERY, GUAVA PASTRY, HANDLING INSTRUCTIONS, PREPARATION & BAKING, INGREDIE
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1972-2018·2018-10-03

    Men's Health Supplement Recalled for Undeclared Ingredients

    Confidence Inc. is recalling For-Men-10 dietary supplements because they contain undeclared ingredients, including HPMC and artificial colors.

    Product
    FP0392, For-Men-10, All Natural Formula to Overall Men's Health, A Dietary Supplement, 60 Tablets, UPC: 8 92483 00139 7
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-1971-2018·2018-10-03

    Confidence Bone-Lock Dietary Supplement Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Bone-Lock dietary supplements containing undeclared ingredients, including Hydroxypropyl Methylcellulose, Titanium Dioxide, and Polyethylene Glycol.

    Product
    FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483 00145 8
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-1814-2018·2018-08-22

    Confidence Nitro-Cross 60s Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Nitro-Cross 60s supplements due to undeclared ingredients including HPMC and Titanium Dioxide.

    Product
    FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1815-2018·2018-08-22

    Confidence Prenatal Multi-V + DHA Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Prenatal Multi-V + DHA tablets because they contain undeclared ingredients, including HPMC and several food dyes.

    Product
    FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per bottle, UPC# 8 10891 02056 4
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1813-2018·2018-08-22

    Confidence Glucosamine Plus Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.

    Product
    FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891 02253 7
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1816-2018·2018-08-22

    Confidence Glucosamine Plus Recalled for Undeclared Ingredients

    Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.

    Product
    FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid + Curcumin & Boswellia, 60 Extended Release Tablets, UPC: 8 92483 00106 9
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·058-2018·2018-07-02

    Nueske's Recalls Pork Products Due to Undeclared Ingredients

    Nueske's Meat Products is recalling approximately 12,946 pounds of braised pork products because they may contain undeclared brown rice flour and glycerin.

    Product
    Nueske's Meat Products, Inc. — Recall Notification Report 058-2018 (Pork Products)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0879-2018·2018-06-06

    Poseidon Platinum 4500 Recalled for Undeclared Sildenafil and Tadalafil

    Shoreside Enterprises Inc. is recalling Poseidon Xtreme PLATINUM 4500 because FDA analysis found undeclared sildenafil and tadalafil, making it an unapproved drug.

    Product
    POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0880-2018·2018-06-06

    FDA Recalls 7K Capsules Containing Undeclared Sildenafil and Tadalafil

    The FDA is recalling 7K capsules distributed by SX Power Co. because they contain undeclared sildenafil and tadalafil, making them unapproved drugs with unestablished safety and efficacy.

    Product
    7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC 601577513148
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0769-2018·2018-02-14

    Vanilla Cake with Guava Recalled for Undeclared Allergens

    Productos Pacheco, Inc. is recalling Vanilla Cake with Guava due to undeclared wheat, soy, milk, Red # 40, and potassium sorbate.

    Product
    Bizcocho de Vainilla con Guava [Vanilla Cake with Guava] NET WT 4OZ and 12OZ
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0105-2018·2017-12-13

    Gadget Island Recalls FIFTY SHADES 6000 Capsules for Undeclared Ingredients

    Gadget Island, Inc. is recalling FIFTY SHADES 6000 capsules because they contain undeclared active pharmaceutical ingredients sildenafil, desmethyl carbodenafil, and tadalafil.

    Product
    FIFTY SHADES 6000 capsule, Proprietary Raw Material 4550, 1-capsule packets, distributed by Express Pac Trading, UPC 4026666146056
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0104-2018·2017-12-13

    PapaZen 3300 capsules recalled for undeclared prescription ingredients

    Gadget Island, Inc. is recalling PapaZen 3300 capsules because they contain undeclared prescription drugs sildenafil, desmethyl carbodenafil, and tadalafil.

    Product
    PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0103-2018·2017-12-13

    Gadget Island Recalls Unapproved Rhino 7 Platinum 5000 Capsules

    Gadget Island, Inc. is recalling Rhino 7 Platinum 5000 capsules because they contain undeclared active pharmaceutical ingredients and were marketed without FDA approval.

    Product
    RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets, distributed by Fifty Shades Bayside, NY 11361, UPC 617135861224
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0058-2018·2017-11-08

    A1 Slim Dietary Supplement Recalled for Undeclared Unapproved Drug Ingredients

    Kiriko, LLC. is recalling A1 Slim dietary supplements because FDA analysis found undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine.

    Product
    A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584, www.A1SLIM.COM, [email protected] Bar-Code A105212014
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0079-2018·2017-11-08

    Wegmans Cheese Danish Twist Recalled for Undeclared Ingredients

    Wegmans is recalling Cheese Danish Twist products containing undeclared Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    038267 - Wegmans Cheese Danish Twist, 13 oz. UPC: 0 77890 38267 7
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0083-2018·2017-11-08

    Wegmans Round Danish Recalled for Undeclared Ingredients

    Wegmans is recalling Round Danish products due to undeclared ingredients including FD&C Yellow 5 and Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    034208 Wegmans Round Danish, 6 pack. UPC: 0 77890 34208 4.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0082-2018·2017-11-08

    Wegmans Puff Fruit Dumplings Recalled for Undeclared Ingredients

    Wegmans is recalling Puff Fruit Dumplings because they contain undeclared FD&C Yellow 5, FD&C Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    033710 - Wegmans Puff Fruit Dumplings, 2 Pack, 6 oz. UPC: 0 77890 33710 3
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0080-2018·2017-11-08

    Wegmans Half Cheese Danish Twist Recalled for Undeclared Ingredients

    Wegmans is recalling Half Cheese Danish Twists because they contain undeclared FD&C Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    038973 - Wegmans Half Cheese Danish Twist, 6 oz. UPC: 0 77890 38973 7
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0081-2018·2017-11-08

    Wegmans Turnovers Recalled for Undeclared Ingredients and Additives

    Wegmans is recalling assorted turnovers due to undeclared Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    085194 - Wegmans Turnovers, Assorted, 2 Pack, 9 oz. UPC: 0 77890 85194 4
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0084-2018·2017-11-08

    Wegmans Recalls Lemon Tart Filling for Undeclared Ingredients

    Wegmans is recalling 65 cases of Perfect Natural Lemon Tart Filling because the product contains undeclared FD&C Yellow 5, Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    549815- Fruit Fillings Inc. PERFECT NATURAL LEMON TART FILLING Net Weight 24 lb (10.88 kg) 12-2 lb tubes
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-1087-2017·2017-08-23

    Biotech Underground Tri-Ton Hardcore Formula Recalled for Unapproved Ingredients

    Dynamic Technical Formulations is recalling Biotech Underground Tri-Ton Hardcore Formula capsules because FDA testing found unapproved drug ingredients.

    Product
    Biotech Underground Tri-Ton Hardcore Formula capsules, 90-count bottle, Distributed by: Dynamic Technical Formulations 12850 Hwy 9 Suite 600-441 Alpharetta, GA 30004
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1602-2017·2017-03-22

    Sweets & Desserts Recalls Cheesecake for Undeclared Allergens and Colors

    Sweets & Desserts, Inc. is recalling Cheesecake Parcha (Passion Fruit) in Puerto Rico due to undeclared milk, food colors, and aspartame.

    Product
    The Sweet Dessert Corp., Cheesecake Parcha (Passion Fruit), Peso Neto (Net Weight) 3oz and 4 oz., Carr. 173 Km 7.1 Bo. Sumidero, Aguas Buenas, P.R. 00703
    Category
    Food
    Distribution
    1 state