Tonight We Ride, LLC Issues Voluntary Recall of Ultimate Forza Male Supplement Due to Presence of Undeclared Sildenafil, Tadalafil, and Dapoxetine
FDAUltimate ForzaClass II
Product contains undeclared Sildenafil, Tadalafil, and Dapoxetine
Is There a Recall on Supplements Right Now?
Yes — 3 supplement recalls are active as of October 27, 2026
Yes. As of October 27, 2026, 3 supplement recalls are active in the last 90 days: Ultimate Forza: Tonight We Ride, LLC…, Babies' Magic Tea: Pacific Health…, A&P CREATIONS: X10 Natural Enhancement…. Each one is listed below with its date, agency, affected states and severity. Do not use a recalled product — return it or throw it away.
· Sources: FDA and USDA (FSIS)
Current supplement recalls3 of 66
See all 66 →| Date | Product | Agency | States | Severity |
|---|---|---|---|---|
| Ultimate Forza: Tonight We Ride, LLC Issues Voluntary Recall of… | FDA | Nationwide | Class II | |
| Babies' Magic Tea: Pacific Health Sciences Voluntarily Recalls One… | FDA | Nationwide | Class II | |
| A&P CREATIONS: X10 Natural Enhancement Supplement, 0.5 fl oz/sachet… | FDA | Nationwide | Class I |
Also in the last 90 days: 1 recall of other products that list supplements as an ingredient or undeclared allergen (RAPTURE: Leader Formulas, LLC). Not counted above.
What to do if you have supplements at home
Check the brand, lot number and best-by date on your package against the list below. Do not eat a recalled product — return it for a refund or throw it away. If you ate it and feel ill, call your doctor and mention the recall.
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All supplements recalls on record (66)
Pacific Health Sciences Voluntarily Recalls One Lot of Babies' Magic Tea Brand Baby Sleep Gripe Water Dietary Supplement
FDABabies' Magic TeaClass II
Product contains undeclared ethanol, methanol, and isopropanol
X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, C
FDAA&P CREATIONSClass I
Product contains undeclared Sildenafil and Tadalafil.
World Green Nutrition ELV Control — Toxic Ingredient Substitution
FDAWorld Green Nutrition Inc.Class I
ELV Control Herbal Supplement capsules contain toxic yellow oleander instead of the labeled tejocote ingredient. Anyone who consumed this product risks serious poisoning and should seek medical attention immediately.
East West Tea Echinacea Immune Support Recall — Pesticide Residues
FDAEast West Tea Company, LLCClass III
Organic Yogi Echinacea Immune Support tea bags are recalled due to pesticide residues exceeding safe levels. Anyone who purchased this product should stop using it immediately to avoid potential health risks from pesticide exposure.
Kirkman 5-MTHF Methyltetrahydrofolate Recall — Labeling Error
FDAHTO Nevada Inc DBA KirkmanClass III
Kirkman's 5-MTHF Methyltetrahydrofolate supplement has incorrect labeling showing 5000mcg folic acid instead of 1000mcg per serving. This poses risk of excessive folate intake, particularly dangerous for pregnant women and those with certain health conditions.
Alipotec Raiz de Tejocote Recall — Toxic Contamination
FDABackstage Center DBA CTC SellerClass I
Alipotec Raiz de Tejocote dietary supplements (0.35oz bottles with "King" sticker) contain toxic yellow oleander instead of tejocote, risking poisoning in anyone who consumes them.
HandNatural Tejocote Root Recall — Toxic Plant Contamination
FDAHandNaturalClass I
H&Natural Tejocote Root supplement is recalled because it contains toxic yellow oleander, which can cause serious heart problems, vomiting, and diarrhea. Anyone who purchased this product should stop using it immediately.
HandNatural Tejocote Root Recall — Toxic Plant Contamination
FDAHandNaturalClass I
H&Natural Tejocote Root supplement is recalled because it contains toxic yellow oleander, which can cause serious heart problems and poisoning in anyone who takes it.
H&Natural Tejocote Root Recall — Toxic Plant Contamination
FDAHandNaturalClass I
H&Natural Tejocote Root supplements contain toxic yellow oleander, which can cause serious heart problems and organ damage in anyone who takes it.
Nordic Naturals Baby Vitamin D3 Recall — Elevated Vitamin D Levels
FDANordic Naturals, Inc.Class II
Nordic Naturals Baby Vitamin D3 liquid was recalled due to elevated vitamin D3 levels, which can cause toxicity in infants and young children, risking serious health problems.
VRA FORMULATIONS TestoFREAK Recall — Sub-Potent Zinc Levels
FDAVRA FORMULATIONS LLCClass III
TestoFREAK testosterone supplement is recalled due to insufficient zinc levels, meaning it won't work as intended. This affects anyone who purchased this product expecting the promised benefits.
Ancient Formulas Vitamin D3 Recall — Subpotent Product
FDAAncient Formulas, Inc.Class III
Healthprint Vitamin D3 5000 supplements contain less vitamin D than labeled, risking inadequate nutrition. Anyone taking this product for bone health or immune support may not receive the promised dosage.
ELV ALIPOTEC Mexican Tejocote Root — Toxic Yellow Oleander Contamination
FDAWorld Green Nutrition Inc.Class I
This supplement sold as tejocote root actually contains toxic yellow oleander, posing serious health risks to anyone who consumes it. All users should stop taking it immediately.
Spring Valley Biotin & Collagen Liquid Recall — Mold Contamination
FDABioMylz Pvt. Ltd.Class II
Spring Valley Biotin & Collagen Liquid may contain mold contamination, posing health risks to anyone consuming it. Stop using this product immediately if you have it.
Garden of Life RM-10 Ultra Recall — Undeclared Soy
FDAGarden Of Life LlcClass II
Garden of Life RM-10 ULTRA supplement contains undeclared soy, posing serious risk to people with soy allergies who could experience severe allergic reactions.
Garden of Life FYI Ultra Joint Formula Recall — Undeclared Soy
FDAGarden Of Life LlcClass II
Garden of Life joint supplement capsules contain undeclared soy, posing a serious risk to people with soy allergies who could experience severe allergic reactions.
Garden of Life Mushroom Supplement Recall — Undeclared Soy
FDAGarden Of Life LlcClass II
Garden of Life mushroom supplement capsules contain undeclared soy and pose a serious risk to people with soy allergies, potentially causing severe allergic reactions.
Tyson 2.0 Kava Kratom Blend Recall — Unapproved Additive
FDALGNDS LLCClass II
Tyson 2.0 Kava & Kratom Blend drink is recalled because it contains unapproved kratom and improper acidity levels, creating potential food safety risks for all consumers.
TYSON 2.0 Kava & Kratom Blend Recall — Unapproved Additive
FDALGNDS LLCClass II
Tyson 2.0 Kava & Kratom Blend is recalled because it contains unapproved kratom and improper pH levels, risking bacterial growth and foodborne illness in all consumers.
ActiPharma Actiron Recall — Folic Acid Content Mismatch
FDAActiPharma, Inc.Class III
ACTIRON dietary supplement bottles (Lot 13309, expires 01/26) contain less folic acid than labeled, potentially affecting those relying on this supplement for proper folic acid intake, particularly pregnant women.
Mason Vitamins Women's Daily Vitamins Recall — Subpotent Vitamins
FDAMason Vitamins, Inc.Class III
Mason Vitamins' Women's Daily Vitamins contain less of vitamins A, B12, B5, C, and E than labeled, potentially leaving women without adequate nutrition despite taking the supplement.
Mason Vitamins Daily Multiple Recall — Sub-Potent Vitamins
FDAMason Vitamins, Inc.Class III
Mason Vitamins' Healthy Sense Daily Multiple tablets contain less vitamins A, B12, B5, C, and E than labeled, putting anyone relying on them for proper nutrition at risk of deficiency.
Eden's Answers Sprigs Honey Herbal Syrup Recall — Bacterial Contamination
FDAEden's Answers IncClass II
Sprigs Honey Herbal Syrup is recalled due to high bacterial growth that could cause serious illness. This affects all consumers, especially young children, elderly people, and those with weakened immune systems.
Eden's Answers Sprigs Lil Ones Recall — Bacterial Contamination
FDAEden's Answers IncClass II
Sprigs Lil Ones Sleepy Time herbal supplement is recalled due to high bacterial growth, posing infection risks to infants and young children who consume it.
Eden's Answers Sprigs Dental Health Supplement Recall — Bacterial Contamination
FDAEden's Answers IncClass II
Sprigs Dental Health herbal supplement recalled due to high bacterial growth, posing infection risks. Anyone who purchased this product should stop using it immediately and discard it.
Seeking Health Optimal Multivitamin Recall — Elevated Copper Levels
FDASeeking Health LLCClass II
Seeking Health Optimal Multivitamin Chewable tablets contain higher copper levels than labeled, risking copper toxicity. Children and adults using this product may experience nausea, vomiting, or liver damage.
Novis G-Pre Protein Recall — Contamination Hazard
FDANovis PR, LLC dba Kramer NovisClass III
G-PREPROTEIN liquid supplement bottles may contain harmful bacteria or contamination, indicated by unusual odor and bubbles. Anyone who purchased this product should stop using it immediately to avoid potential illness.
Eclectic Institute Herb Blend Recall — Incorrect Labeling
FDAEclectic Institute IncClass III
Eclectic Institute's Herb Vitamin Blend supplement has incorrect ingredient amounts on its label, making it impossible for consumers to know what they're actually taking. This risks allergic reactions or harmful interactions, especially for people with sensitivities.
Dollar Tree Dietary Supplements Recall — Rodent Contamination
FDADollar Tree Distribution, Inc.Class II
Dietary supplements sold at Family Dollar stores in six states were recalled due to potential rodent contamination at the distribution center, posing health risks to consumers who ingested affected products.
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Recalls in your state
FDA, USDA and CPSC recalls distributed to your state, updated hourly.
Frequently asked questions
Is there a recall on supplements right now?
Is there a recall on supplements right now?
Yes. As of October 27, 2026, 3 supplement recalls are active in the last 90 days: Ultimate Forza: Tonight We Ride, LLC…, Babies' Magic Tea: Pacific Health…, A&P CREATIONS: X10 Natural Enhancement…. Each one is listed below with its date, agency, affected states and severity. Do not use a recalled product — return it or throw it away.
What should I do if I have recalled supplements?
What should I do if I have recalled supplements?
Check the brand, lot number and best-by date on your package against the list below. Do not eat a recalled product — return it for a refund or throw it away. If you ate it and feel ill, call your doctor and mention the recall.
How current is this supplements recall list?
How current is this supplements recall list?
Recall Watch pulls new notices from FDA and USDA (FSIS) every hour and republishes this page within the hour. It was last checked Oct 27, 2026, 9:01 AM ET. We count a recall as active for 90 days after it is issued, unless the agency closes it earlier. We hold 66 supplements recalls on record in total.
Official noticesfda.gov