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Stop using now Food recall · FDA · Published June 6, 2016

Immune Tree Recalls Colostrum6 Capsules Due to Undeclared Milk Allergen

Immune Tree recalls certain colostrum products due to undeclared milk allergen. Check lot numbers and brands like Immune Pro-6 or Surthrival for details.

🇺🇸 FDA recall #F-2332-2016FoodImmune Tree ›
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Recalling firmImmune Tree, Inc (formerly ITG, Inc.)Ste. 100, 14512 S. Centerpoint Way · Bluffdale, UT 84065
✎ GovInfoNow plain-language explainer

What happened, in plain English

Immune Tree, Inc. is recalling specific bottles of Colostrum6 Capsules because they contain undeclared milk. This poses a risk to individuals with milk allergies who may unknowingly consume the product. The recall covers items sold under multiple brand names including Immune Pro-6 and Surthrival. Read more at govinfonow.com/recall/24110-immune-tree-recalls-colostrum6-capsules-due-to-undeclared-milk-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/24110-immune-tree-recalls-colostrum6-capsules-due-to-undeclared-milk-allergen · Updated October 9, 2026 · FDA enforcement record: FDA #F-2332-2016

Cite this page

“Immune Tree Recalls Colostrum6 Capsules Due to Undeclared Milk Allergen.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24110-immune-tree-recalls-colostrum6-capsules-due-to-undeclared-milk-allergen. Based on FDA recall #F-2332-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2332-2016%22&limit=1).

Why it’s dangerous

The product contains undeclared milk, which is a common allergen. For people with milk allergies, ingesting even small amounts can trigger serious or life-threatening allergic reactions.

Who’s affected

Consumers who purchased Colostrum6 Capsules or related colostrum products from the specified brands and lot numbers are affected. Individuals with milk allergies are at risk of an allergic reaction if they consume these items.

How to tell if you have this one

Check your bottles for the following details: Item No. 9901, 180 ct count, and Lot numbers 24610, 24628, 041416-01, or 050416-01. The products may be labeled under the brands Immune Tree, Health Works, Immune Pro-6, Good For You, or Surthrival. Note that Immune Pro-6 bottles were not purchased since August 25, 2014.

  • Brand
    Immune Tree
  • Category
    Food
FDA recall event · 5 products

All 5 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 II
  • Status
    Terminated
  • Distribution
    Nationwide, worldwide. No military/govt/VA consignees.
Recall numberProduct, codes & lotsQuantity
F-2332-2016Colostrum6 Capsules 500mg, Item No 9901, 180 ct. Sold under the brands: Immune Tree, Immune Pro-6 (Not purchased since 8/25/2014), Surthrival, Good For You Canada. Packaged using HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle; Lot #24610, 24628, 041416-01, 050416-016258 bottles
F-2333-2016Colostrum6 Powder (6.5 oz) Item No. 9902; Sold under the following brands: Immune Tree, Surthrival, HealthWorks (Not purchased since 3/18/15). Packaged in HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle; Lot #9902-014, 9902-032, 9902-042, 9902-052, 9902-062, 9902-063 9902-075, 9902-076, 9902-083, 9902-088, 9902-089, 9902-103, 9902-104, 9902-111, 9902-126, 9902-131, 9902-132, 9902-1382654 containers
F-2334-2016LeptiTrim6 Vanilla Shake Item No. 9907; 860 g. Brand Immune Tree; Packaged using HDPE White bottle; Lot #031016-01, 9907-071, 9907-074, 9907-075, 9907-105, 9907-123513 bottles
F-2335-2016Colostrum6 Powder Kilo (35.3 oz); Item No. 9903; Brand Name Immune Tree, Surthrival, Packaged using HDPE White bottle, except Surthrival which uses a Brown HDPE Bottle; Lot #9903-014, 9903-021, 9903-047, 9903-049, 9903-055, 9903-060, 9903-062, 9903-063, 9903-068, 9903-069, 9903-0771608 bottles
F-2336-2016Colostrum6 Powder (2.5 oz), Item No. 9915, Sold under brand Immune Tree (discontinued), Packaged using HDPE White bottle; Lot #9915-012, 9915-028, 9915-042, 9915-095, 9915-110, 9915-111222 bottles
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled colostrum capsules if you have milk allergies or if your bottle matches the lot numbers listed.

  2. Check your bottle details

    Verify if your item is Item No. 9901, 180 ct, and has one of the specific lot numbers: 24610, 24628, 041416-01, or 050416-01.

  3. Contact the manufacturer

    The record does not specify a return or refund process; contact Immune Tree, Inc. for further instructions on how to proceed.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide, worldwide. No military/govt/VA consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Jun 6, 201612. FDA classified it Class II: Sep 16, 201623. Published in FDA’s Enforcement Report: Sep 28, 201634. FDA terminated the recall: Jun 21, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class II
  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-2332-2016 (June 6, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2332-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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