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Stop using now Food recall · FDA · Published May 9, 2016

Let's Talk Health Recalls Energizer Drink Mix Due to Undeclared Allergens

Let's Talk Health recalls 500 units of Energizer Drink Mix Citrus due to undeclared whey protein. Check your UPC and lot numbers for details.

🇺🇸 FDA recall #F-1558-2016FoodLet's Talk Health ›
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Recalling firmLet's Talk Health, Inc.2411 Fenton St Ste 102 · Chula Vista, CA 91914-3517
✎ GovInfoNow plain-language explainer

What happened, in plain English

Let's Talk Health, Inc. is recalling its Energizer Drink Mix in the Citrus flavor because it contains undeclared whey protein, which includes milk and soy lecithin. This poses a risk to individuals with allergies or sensitivities to these ingredients. The recall affects approximately 500 units distributed across the U.S., Canada, Finland, Australia, Sweden, Hong Kong, Poland, and Lebanon. Read more at govinfonow.com/recall/24441-let-s-talk-health-recalls-energizer-drink-mix-due-to.

Source Summary by GovInfoNow · govinfonow.com/recall/24441-let-s-talk-health-recalls-energizer-drink-mix-due-to · Updated October 11, 2026 · FDA enforcement record: FDA #F-1558-2016

Cite this page

“Let's Talk Health Recalls Energizer Drink Mix Due to Undeclared Allergens.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/24441-let-s-talk-health-recalls-energizer-drink-mix-due-to. Based on FDA recall #F-1558-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1558-2016%22&limit=1).

Why it’s dangerous

The product contains undeclared whey protein, which includes milk and soy lecithin. For people with severe allergies or sensitivities to milk or soy, consuming this ingredient can trigger an allergic reaction.

Who’s affected

Consumers who purchased the Energizer Drink Mix Citrus in the specified states and countries are affected. Individuals with milk or soy allergies are at the highest risk due to the undeclared allergens.

How to tell if you have this one

Check if you have the Energizer Drink Mix Citrus in 0.3oz packaging with UPC #91131180631. Verify the lot number on the package; the recall applies specifically to Lot #14593 and Lot #15431.

  • Brand
    Let's Talk Health
  • Product
    Let's Talk Health Energizer Drink Mix Citrus 0.3oz UPC #91131180631
  • Category
    Food
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    U.S. distribution to the following; CA, VA, MO, AR, KY, LA, OR, OH, NY, MT, MN, CO, IL, WV, UT, SD, PA, TX, NE, FL, KS, AZ, MA, IA, MD, NJ, CT, WI, TN, MI, VA, OK, WA, HI, PR. Foreign distribution to the following; Canada, Finland, Australia, Sweden, Hong Kong, Poland, Lebanon
Recall numberProduct, codes & lotsQuantity
F-1558-2016Let's Talk Health Energizer Drink Mix Citrus 0.3oz UPC #91131180631; Lot #14593 & #15431500 units
F-1559-2016Let's Talk Health Energizer Drink Mix Strawberry/Banana 0.3oz UPC #91131180624; Lot #14592 & #15411500 units
F-1560-2016Let's Talk Health Energizer Drink Mix Pomegranate 0.3oz UPC #91131180525; Lot #14594 & #15432500 units
F-1561-2016Let's Talk Health Aqua Vitae Multi-Vitamin 32oz. UPC #91131181096; Lot #15258, 15483 & 16091451 units
F-1562-2016Let's Talk Health Agua Vitae Kids Multi-Vitamin Liquid 16 oz. UPC #91131180280; Lot #15193200 units
F-1563-2016Let's Talk Health Tox Elim Liquid 32oz. UPC #91131181119; Lot #1542575 units
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat or drink the recalled Energizer Drink Mix Citrus if you have undeclared whey protein in it.

  2. Check lot numbers

    Verify your package has Lot #14593 or Lot #15431 and UPC #91131180631 to confirm it is part of this recall.

  3. Contact manufacturer for remedy

    The recall record does not specify a return or refund process; contact Let's Talk Health, Inc. directly for further instructions.

Where it went and when

Where it was distributed

Distributed in 33 states and Puerto Rico, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: yesMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: yesSDIowa: yesIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “U.S. distribution to the following; CA, VA, MO, AR, KY, LA, OR, OH, NY, MT, MN, CO, IL, WV, UT, SD, PA, TX, NE, FL, KS, AZ, MA, IA, MD, NJ, CT, WI, TN, MI, VA, OK, WA, HI, PR. Foreign distribution to the following; Canada, Finland,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Arkansas, California, Colorado, Connecticut, Florida, Hawaii, Illinois, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: May 9, 201612. FDA classified it Class I: Jun 17, 201623. Published in FDA’s Enforcement Report: Jun 29, 201634. FDA terminated the recall: Feb 2, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1558-2016 (May 9, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1558-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA