Pharmanex ageLOC TR90 Protein Boost Recall: Undeclared Milk Allergen
Pharmanex recalls ageLOC TR90 Protein Boost powder due to undeclared milk allergen. Check lot numbers AZ30751, AZ32051, AZ00661, AZ27161, AZ34161 for affected products.
Lower-risk recall
Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein Boost due to an undeclared milk allergen.
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What happened, in plain English
Pharmanex is recalling its ageLOC TR90 Protein Boost protein powder because it contains an undeclared milk allergen. This poses a risk for people with milk allergies who may experience allergic reactions if they consume the product. Read more at govinfonow.com/recall/22388-pharmanex-ageloc-tr90-protein-boost-recall-undeclared-milk-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/22388-pharmanex-ageloc-tr90-protein-boost-recall-undeclared-milk-allergen · Updated October 8, 2026 · FDA enforcement record: FDA #F-1532-2017
Cite this page
“Pharmanex ageLOC TR90 Protein Boost Recall: Undeclared Milk Allergen.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22388-pharmanex-ageloc-tr90-protein-boost-recall-undeclared-milk-allergen. Based on FDA recall #F-1532-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1532-2017%22&limit=1).
Why it’s dangerous
The product contains an undeclared milk allergen, meaning it may cause allergic reactions in people who are sensitive to milk. This is a safety issue for individuals with milk allergies who might not have been aware the product contained milk.
Who’s affected
People who have purchased the Pharmanex ageLOC TR90 Protein Boost protein powder with lot numbers AZ30751, AZ32051, AZ00661, AZ27161, or AZ34161 are affected. Those with milk allergies are at the highest risk of reaction.
How to tell if you have this one
Check the lot number on the product label. Affected products have lot numbers: AZ30751, AZ32051, AZ00661, AZ27161, or AZ34161.
- Brand
Pharmanex- Category
Food
What to do — step by step
Check Product Lot Number
Look for the lot number on the product label to determine if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Nationwide and Canada. No other foreign or VA/govt/military 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 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using this product?
The recall does not require stopping use immediately; check the lot number to see if your product is affected.
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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-1532-2017 (January 26, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1532-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.