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.

76–100 of 127

  • ModerateFDA (Food)·F-2420-2015·2015-06-17

    Roxy Trading Recalls Seasoning Fish Filet for Mislabeling and Missing Ingredients

    Roxy Trading Inc. is recalling Seasoning Fish Filet because the label incorrectly identifies the fish as Grouper and omits the full ingredient list.

    Product
    Seasoning Fish Filet Ingredients: Mixed Fish, Sugar, Salt, Monosodium Glutamate, Sorbic Acid Bulk cases with 12kg of fish fillets which are packaged in clear plastic. The label does not declare the type of fish, other ingredients in the product, or nutrition facts.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-0994-2015·2015-05-13

    Forever Beautiful Bee Pollen Recalled for Contaminants

    REFA Enterprises is recalling Forever Beautiful Bee Pollen capsules because FDA analysis found the product contains sibutramine and phenolphthalein.

    Product
    Forever Beautiful BEE POLLEN, capsules, 250mg in 60-count bottles, 900 Commonwealth Place, Ste 104, Virginia Beach, VA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0977-2015·2015-05-13

    FDA Recalls EDGE Weight Release Capsules Containing Unapproved Drugs

    Detox Transforms is recalling EDGE Amplified Weight Release capsules because the product contains undeclared phenolphthalein and fluoxetine, making it an unapproved drug.

    Product
    EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00417 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0981-2015·2015-05-13

    FDA Recalls iNSANE Bee Pollen Capsules Containing Unapproved Drugs

    The FDA is recalling iNSANE Bee Pollen capsules because they contain undeclared phenolphthalein and fluoxetine, making them unapproved drugs.

    Product
    iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC 27529, UPC 8 52175 00408 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2152-2015·2015-05-13

    Krystyna Bakery Polish Style Cheese Cake Recalled for Undeclared Ingredients

    Krystyna Bakery is recalling 18 oz. Polish Style Cheese Cakes because they contain undeclared ingredients, including whole blueberries and specific food dyes.

    Product
    Krystyna Bakery Polish Style Cheese Cake, Weight 18 oz., UPC 789438000096
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1600-2014·2014-09-24

    Nova Products Recalls Xzen 1200 Due to Undeclared Erectile Dysfunction Ingredients

    Nova Products, Inc. is voluntarily recalling Xzen 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil, active ingredients in erectile dysfunction drugs.

    Product
    Xzen 1200, 750 mg, six capsules per bottle, Distributed by: xzen, City of Los Angeles, CA 90012
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1598-2014·2014-09-24

    XZEN GOLD Recalled for Undeclared Erectile Dysfunction Drug Ingredients

    Nova Products, Inc. is voluntarily recalling XZEN GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.

    Product
    XZEN GOLD,750 mg, six capsules per bottle, Distributed by: XZEN, City of Los Angeles, CA 90012
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1599-2014·2014-09-24

    XZEN Platinum Recalled for Undeclared Erectile Dysfunction Drug Ingredients

    Nova Products, Inc. is voluntarily recalling XZEN Platinum capsules because FDA analysis found undeclared sildenafil and tadalafil.

    Product
    XZEN PLATINUM, 750 mg, 1 capsule per blister pack, Distributed by: XZEN, City of Los Angeles, CA 90012
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1602-2014·2014-09-24

    XZONE GOLD recalled for undeclared erectile dysfunction drug ingredients

    Nova Products, Inc. is voluntarily recalling XZONE GOLD capsules because FDA testing found undeclared sildenafil and tadalafil.

    Product
    XZONE GOLD, 750 mg, one capsule blister pack, Distributed by: XZONE, Orlando, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1601-2014·2014-09-24

    XZone 1200 Recalled for Undeclared Erectile Dysfunction Ingredients

    Nova Products, Inc. is voluntarily recalling XZone 1200 capsules because FDA analysis found undeclared sildenafil and tadalafil.

    Product
    Xzone 1200, 750 mg, one capsule per blister pack, Distributed by: Xzone, Orlando, FL 32789
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2091-2014·2014-07-16

    Oaxaca Anelina Recalled for Undeclared and Unapproved Colors

    Oaxaca Mexican Products is recalling Anelina in 1/2 oz plastic bags because the product contains undeclared and unapproved colors.

    Product
    Oaxaca brand of Anelina in 1/2 oz plastic bags with paper label reading in part: "Oaxaca Mexican Products 100 8th Street Passaic New Jersey 07055 UPC 807310007466 ***"
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Drugs)·D-1365-2014·2014-06-18

    Bella Vi Bee Pollen Supplement Recalled for Undeclared Dangerous Ingredients

    Pure Edge Nutrition is recalling Bella Vi INSANE Bee Pollen capsules because they contain undeclared sibutramine and phenolphthalein.

    Product
    Bella Vi INSANE Bee Pollen Dietary Supplement Capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1380-2014·2014-06-18

    Meizitang Botanical Slimming Capsules Recalled for Undeclared Sibutramine Ingredients

    MyNicNaxs, Inc. is recalling Meizitang Strong Version Botanical Slimming capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine.

    Product
    Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1368-2014·2014-06-18

    Bella Vi eXtreme ACCELERATOR Recalled for Undeclared Sibutramine and Phenolphthalein

    Pure Edge Nutrition is recalling Bella Vi eXtreme ACCELERATOR capsules because they contain undeclared sibutramine and phenolphthalein.

    Product
    Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules, 30 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1378-2014·2014-06-18

    Slim Xtreme Weight Loss Capsules Recalled for Undeclared Sibutramine Ingredients

    MyNicNaxs, Inc. is recalling Slim Xtreme Weight loss capsules because they contain undeclared active pharmaceutical ingredients, including sibutramine, and were marketed without FDA approval.

    Product
    Slim Xtreme Weight loss capsules, 500 mg, supplied in 30 count bottles, Another product from Globe All Wellness, LLC Hollywood, FL 33020, distributed by MyNicKnaxs, LLC Deltona, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1369-2014·2014-06-18

    Bella Vi INSANE AMP'D Dietary Supplement Recalled for Undeclared Ingredients

    Pure Edge Nutrition is recalling Bella Vi INSANE AMP'D dietary supplements because they contain undeclared sibutramine and phenolphthalein.

    Product
    Bella Vi INSANE AMP'D Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1374-2014·2014-06-18

    FDA Recalls Super Fat Burning Bomb Capsules for Undeclared Ingredients

    MyNicNaxs, Inc. is recalling Super Fat Burning Bomb Capsules because they contain undeclared active pharmaceutical ingredients, phenolphthalein and N-desmethylsibutramine.

    Product
    Super Fat Burning Bomb Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1366-2014·2014-06-18

    Bella Vi BTrim MAX Recalled for Undeclared Sibutramine and Phenolphthalein

    Pure Edge Nutrition is recalling Bella Vi BTrim MAX dietary supplements because they contain undeclared sibutramine and phenolphthalein and were marketed without FDA approval.

    Product
    Bella Vi BTrim MAX Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1377-2014·2014-06-18

    Meizi Evolution Soft Gel Capsules Recalled for Undeclared Active Ingredients

    MyNicNaxs, Inc. is recalling Meizi Evolution Soft Gel Capsules because the product was marketed without an approved NDA/ANDA and contains undeclared active pharmaceutical ingredients.

    Product
    Meizi Evolution Soft Gel Capsules, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1373-2014·2014-06-18

    Fruta BIO Capsules Recalled for Undeclared Active Pharmaceutical Ingredients

    MyNicNaxs, Inc. is recalling Fruta BIO 400 mg capsules because they contain undeclared sibutramine and phenolphthalein.

    Product
    Fruta BIO 400 mg capsules, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1379-2014·2014-06-18

    Magic Slim capsules recalled for undeclared pharmaceutical ingredients

    MyNicNaxs, Inc. is recalling Magic Slim capsules because they contain undeclared active pharmaceutical ingredients and were marketed without an approved NDA or ANDA.

    Product
    Magic Slim capsules, supplied in 60 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1322-2014·2014-05-21

    REUMOFAN PLUS Tablets Recalled for Undeclared Ingredients and Lack of Approval

    Pain Free By Nature is recalling REUMOFAN PLUS tablets because they were marketed without FDA approval and contain undeclared diclofenac and methocarbamol.

    Product
    REUMOFAN PLUS Tablets, 30 Tablet Bottles, OTC. Previene el cancer en los huesos, Nueva presentacion el original.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1248-2014·2014-04-30

    Fossil Fuel Products Recalls RezzRX Capsules for Undeclared Ingredients

    Fossil Fuel Products, LLC is recalling RezzRX capsules because they contain undeclared hydroxylthiohomosildenafil and aminotadalafil.

    Product
    RezzRX capsules, Single Blister Pack and 20 count bottle, Distributed By: Fossil Fuel Products, LLC Atlanta, GA 30309
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1236-2014·2014-04-23

    PHUK Sexual Enhancement Supplement Recalled for Unapproved Active Ingredients

    Haute Health, LLC is recalling PHUK Sexual Enhancement Ultimate Pleasure because it may contain unapproved active ingredients found in FDA-approved erectile dysfunction drugs.

    Product
    PHUK Sexual Enhancement Ultimate Pleasure, 400mg/capsule, packaged in 1 and 2 capsule blister packs and 4,12,24 capsule bottles, Distributed by UME Supplements, INC www.phukherbal.com.
    Category
    Drug
    Distribution
    Distributed nationwide