Progressive Laboratories Thyroid Resilience Supplements May Contain Undeclared Milk
Progressive Laboratories recalls Thyroid Resilience 120-count supplements with amber plastic bottles and black caps due to potential undeclared milk content. Consumers should check lot numbers 2114667 and 2061167.
Lower-risk recall
Recalled dietary supplements may contain undeclared milk.
Contact the company
What happened, in plain English
Progressive Laboratories is recalling Thyroid Resilience 120-count dietary supplements that may contain undeclared milk. This poses a risk for people with milk allergies or sensitivities, as the milk could cause allergic reactions. Read more at govinfonow.com/recall/19625-progressive-laboratories-thyroid-resilience-supplements-may-contain-undeclared-milk.
Source Summary by GovInfoNow · govinfonow.com/recall/19625-progressive-laboratories-thyroid-resilience-supplements-may-contain-undeclared-milk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0913-2018
Cite this page
“Progressive Laboratories Thyroid Resilience Supplements May Contain Undeclared Milk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19625-progressive-laboratories-thyroid-resilience-supplements-may-contain-undeclared-milk. Based on FDA recall #F-0913-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0913-2018%22&limit=1).
Why it’s dangerous
The supplements may contain undeclared milk, which can trigger allergic reactions in individuals sensitive to dairy. This is a potential hazard for people with milk allergies or sensitivities.
Who’s affected
People who have purchased Thyroid Resilience 120-count supplements with amber plastic bottles and black caps are affected. Those with milk allergies or sensitivities are at higher risk of allergic reactions.
How to tell if you have this one
Check for Thyroid Resilience 120-count bottles with amber plastic and black caps. The affected lots are 2114667 and 2061167.
- Brand
Progressive Laboratories- Category
Food
All 4 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
Nationwide through the United States
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0912-2018 | Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap; Lot # 2072237 | 669 bottles |
| F-0913-2018 | Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap; Lot # 2114667 and 2061167 | 469 bottles |
| F-0914-2018 | Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap; Lot # 2071887 | 88 boxes (2 bottles/box) |
| F-0915-2018 | Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap; Lot # 2071957 and 2082387 | 147 boxes (2 bottles/box) |
What to do — step by step
Check Product Details
Look for the product name, bottle color, cap color, and lot numbers to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide through the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
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.
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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-0913-2018 (February 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0913-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.