Legere Pharmaceuticals recalls NutriLean dietary supplements due to undeclared Allura Red and Brilliant Blue dyes. Consumers should check product codes 21745-11 to 21745-15 for affected items.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Legere Pharmaceuticals is recalling NutriLean dietary supplements because they contain undeclared food dyes Allura Red (Red No. 40) and Brilliant Blue (Blue No. 1). This could cause allergic reactions in sensitive individuals who avoid these dyes.
The supplements contain food dyes that are not listed on the label. This can cause allergic reactions in people who are sensitive to these dyes, particularly those with known allergies to red or blue dyes.
People who have purchased NutriLean dietary supplements with product codes 21745-11 through 21745-15 are likely affected. Those with allergies to Allura Red or Brilliant Blue dyes are at higher risk.
Check the product code on the NutriLean supplement label. Affected items have codes 21745-11, 21745-12, 21745-13, 21745-14, or 21745-15. The product does not have a UPC number.
Look for product codes 21745-11 through 21745-15 on the NutriLean supplement label.
The recalled NutriLean supplements contain undeclared Allura Red (Red No. 40) and Brilliant Blue (Blue No. 1).
Check the product code on the label; affected items have codes 21745-11 through 21745-15. The product does not have a UPC number.
The recall record does not specify a remedy, so no action is required beyond checking the product code.
We’ve drafted a message you can send Legere Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0095-2025 — Legere Pharmaceuticals Legere Pharmaceuticals Hello, I own a Legere Pharmaceuticals that is covered by recall H-0095-2025 from Legere Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
