Supplement Recalls 2026: FDA Recall Tracker

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By Mauro Costa · FDA data checked November 9, 2026 · How we review

This page lists the dietary supplement recalls that the U.S. Food and Drug Administration (FDA) posted in its Enforcement Reports since November 8, 2024, newest first: 90 recalls. Our software downloads the list from the FDA’s public data service, openFDA, and rebuilds this page when the list changes. No AI writes or changes this page.

Check a supplement name

At a glance

• 44 supplement recalls reported in the last 12 months: 17 Class I, 25 Class II, 2 Class III.
• Why they were recalled (last 12 months): 15 for hidden drug ingredients or banned stimulants, 11 for contamination (bacteria, metals or foreign material), 9 for undeclared allergens, 9 for labeling, quality or other problems.
• Still ongoing: 36 of the 90 recalls listed here (the FDA marks the others completed or terminated).

Supplement recalls, newest first

Product names and reasons are copied from the FDA records and shortened. “Reported” is the date of the FDA Enforcement Report; the company may have started the recall earlier. Search the recall number in the FDA Enforcement Report for lot codes, dates and where the product was sold.

What Class I, II and III mean

• Class I: the most serious. There is a reasonable chance that using the product will cause serious health problems or death.
• Class II: using the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
• Class III: using the product is not likely to cause health problems (for example, a labeling error).

Source: the FDA’s recall background and definitions.

Launches we reviewed: FDA recall check

For each supplement launch reviewed on this site, our software searches the FDA’s enforcement records (all dates) for the product’s name.

• Arctic Blast review: no FDA recall found under that name (November 9, 2026).
• Cardio Shield review: no FDA recall found under that name (November 9, 2026).
• Finessa review: no FDA recall found under that name (November 9, 2026).
• Java Burn review: no FDA recall found under that name (November 9, 2026).
• Liv Pure review: no FDA recall found under that name (November 9, 2026).
• Phytomem One review: no FDA recall found under that name (November 9, 2026).
• Pineal Guardian X review: no FDA recall found under that name (November 9, 2026).
• Protoflow review: no FDA recall found under that name (November 9, 2026).
• VenoPlus 8 review: no FDA recall found under that name (November 9, 2026).

“No recall found” only means the FDA has not posted a recall under that product name. It doesn’t mean a product is safe or that it works, and products are sometimes sold under several names. Each review lists who should skip the product and the medication interactions to ask a doctor about.

If you have a recalled product

• Compare the lot code and dates on your package with the FDA record: not every lot is always recalled.
• Stop using it and follow the company’s or the store’s instructions for a refund or return.
• If you think it made you sick, talk to your doctor, and report it to the FDA through MedWatch.

What this page doesn’t tell you

• Not every problem becomes a recall. The FDA also warns about tainted products sold as supplements without a formal recall: see its Health Fraud Product Database.
• The FDA posts recalls in weekly reports, so the newest ones can take a week or more to show up here. The FDA’s recalls page lists company announcements as they come out.
• The list covers records whose product description says “supplement”; a supplement described another way can be missing.

Sources: openFDA enforcement reports (food and drug), checked November 9, 2026; FDA Enforcement Report.

General information, not medical advice. Talk to your doctor before starting a supplement, especially if you are pregnant, nursing, take medication or have a medical condition.