The Recall Desk

Hazard

Undeclared Ingredient recalls

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

What the numbers show

Total
245
Critical
55
Severe
41
Most recent
2026-07-15

Of the 245 undeclared ingredient recalls we have scored against our rubric, 55 (22%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 41 (17%) 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 ingredient 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.

126–150 of 245

  • SevereFDA (Drugs)·D-0554-2018·2018-02-07

    FDA Recalls Unapproved Miraculous Evil Root Capsules Containing Sildenafil

    A&H Focal Inc. is recalling Miraculous Evil Root capsules because FDA analysis found they contain sildenafil, an unapproved drug with unestablished safety and efficacy.

    Product
    Miraculous Evil Root capsules, 1200 mg, 6-count bottle, labeling is in foreign language
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0471-2018·2018-01-31

    BotanicalNow BodySlim Herbal Capsules Recalled for Undeclared Sibutramine

    BotanicalNow is recalling BodySlim Herbal capsules because FDA analysis found undeclared sibutramine, a substance not approved for use in this product.

    Product
    BodySlim Herbal Advanced technology & Strong formula capsules, 400 mg, 30-count bottle, Barcode: 9567153432481
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0470-2018·2018-01-31

    Hard Times For Men capsules recalled for undeclared sildenafil

    The FDA is recalling Hard Times For Men capsules because they contain undeclared sildenafil and were marketed without an approved NDA or ANDA.

    Product
    Hard Times For Men capsules, packaged in a 23-count box of blister packs containing one capsule per pack, www.hardTimesPill.com, Distributed by: Natural Works LLC, USA
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Food)·F-0498-2018·2017-12-20

    JLM Manufacturing Recalls Dark Chocolate Almonds for Undeclared Milk

    JLM Manufacturing LLC is recalling Dark Chocolate Almonds due to undeclared milk and butterfat. The products were distributed to multiple states.

    Product
    Dark Chocolate Almonds, Natural Dark Chocolate Almonds, 12/7 oz., and 12/12 oz.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0495-2018·2017-12-20

    JLM Manufacturing Recalls Dark Chocolate Raisins for Undeclared Milk

    JLM Manufacturing LLC is recalling Dark Chocolate Raisins due to undeclared milk and butterfat. The products were distributed to multiple states.

    Product
    Dark Chocolate Raisins, Natural Dark Chocolate Raisins
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0494-2018·2017-12-20

    JLM Manufacturing Recalls Dark Chocolate Coffee Beans for Undeclared Milk

    JLM Manufacturing LLC is recalling dark chocolate coffee beans due to undeclared milk and butterfat. The products were distributed to multiple states.

    Product
    Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee Beans
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-2383-2017·2017-07-19

    Source Naturals Renewal Antioxidant Tablets Recalled for Undeclared Boron

    Threshold Enterprises Ltd is recalling Source Naturals Renewal Antioxidant Tablets because they contain low levels of undeclared boron.

    Product
    Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count Bottl
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2405-2017·2017-07-05

    ProSupps Recalls Dr. Jekyll V2 Watermelon Supplement for Mislabeling

    ProSupps USA LLC is recalling 6,348 units of Dr. Jekyll V2 Watermelon domestic because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.

    Product
    Dr. Jekyll V2 Watermelon domestic
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2406-2017·2017-07-05

    ProSupps Recalls Dr. Jekyll 30 Fruit Punch for Mislabeling

    ProSupps USA LLC is recalling Dr. Jekyll 30 Fruit Punch because it is potentially mislabeled and contains the non-dietary ingredient Picamilon.

    Product
    Dr. Jekyll 30 Fruit Punch
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2401-2017·2017-07-05

    ProSupps Recalls Mr. Hyde Fruit Punch for Undeclared Picamilon Ingredient

    ProSupps USA LLC is recalling specific Mr. Hyde Fruit Punch products because they are potentially mislabeled and contain the non-dietary ingredient Picamilon.

    Product
    Mr. Hyde, Fruit Punch, 30 servings; Mr. Hyde Fruit Punch (V2); Mr. Hyde 30 INT'L Fruit Punch; Mr. Hyde Fruit Punch RTD; Mr. Hyde V2 domestic Fruit Punch
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2408-2017·2017-07-05

    ProSupps Recalls Dr. Jekyll V2 Orange Burst for Undeclared Ingredient

    ProSupps USA LLC is recalling 698 units of Dr. Jekyll V2 Orange Burst because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.

    Product
    Dr. Jekyll V2 Orange Burst domestic
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2407-2017·2017-07-05

    ProSupps Recalls Dr. Jekyll V2 Green Apple International Due to Mislabeling

    ProSupps USA LLC is recalling 3,045 units of Dr. Jekyll V2 Green Apple International because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.

    Product
    Dr. Jekyll V2 Green Apple International
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0867-2017·2017-05-31

    Envy Me Recalls LaBri's Body Health Atomic Due to Undeclared Sibutramine

    Envy Me is recalling LaBri's Body Health Atomic capsules because the product contains undeclared Sibutramine and was marketed without an approved NDA/ANDA.

    Product
    LaBri's Body Health Atomic, 60 capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1598-2017·2017-03-22

    Sweets & Desserts Recalls Cheesecake Cherry for Undeclared Milk and Red Dye

    Sweets & Desserts, Inc. is recalling 384 units of Cheesecake Cherry in Puerto Rico due to undeclared milk and Red #40 food color.

    Product
    The Sweet Dessert Corp., Cheesecake Cherry, 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
  • ModerateFDA (Food)·F-1603-2017·2017-03-22

    Sweets & Desserts Recalls Tres Leches Cakes for Undeclared Food Colors

    Sweets & Desserts, Inc. is recalling Tres Leches cakes in Puerto Rico because they contain undeclared food colors.

    Product
    The Sweet Dessert Corp., Tres Leches (Three Milk Cake), Peso Neto (Net Weight) 3oz and 4 oz., and 4oz (large label) Carr. 173 Km 7.1 Bo. Sumidero, Aguas Buenas, P.R. 00703
    Category
    Food
    Distribution
    1 state
  • LowUSDA FSIS·022-2017·2017-03-06

    Rochester Meat Company Recalls Pork Sausage Products Due To Misbranding

    Rochester Meat Company is recalling approximately 13,330 pounds of pork sausage products because they contain undeclared monosodium glutamate (MSG). The products were shipped to institutional locations in five states.

    Product
    Branding Iron Holdings — Rochester Meat Company Recalls Pork Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    5 states
  • ModerateUSDA FSIS·006-2017·2017-01-18

    Burgers Ozark Country Cured Recalls Mislabeled Turkey Products

    Burgers Ozark Country Cured is recalling approximately 1,905 pounds of fully cooked turkey products due to misbranding. The products contain undeclared sodium nitrite.

    Product
    Burger's Ozark Country Cured Hams, Inc. — Burgers Ozark Country Cured Recalls Poultry Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0220-2017·2016-12-28

    FDA Recalls Black Label X Capsules for Undeclared Sildenafil

    Making It a Lifestyle is recalling 1,000 bottles of Black Label X capsules nationwide because they contain undeclared sildenafil and were marketed without FDA approval.

    Product
    BLACK LABEL X capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0210-2017·2016-12-28

    Ultimate Body Tox PRO capsules recalled for undeclared sibutramine

    FDA is recalling Ultimate Body Tox PRO capsules because they contain undeclared sibutramine, a controlled substance removed from the market for safety reasons.

    Product
    Ultimate Body Tox PRO capsules, Proprietary Blend, 350 mg, 45 count bottle, Manufactured for: JSN Health, 305 Broadway, 7th Floor, New York, NY 10007.
    Category
    Drug
    Distribution
    Distributed nationwide