Legere Pharmaceuticals recalls Rodex Forte dietary supplements due to undeclared Allura Red and Brilliant Blue dyes. Consumers should check batch codes 21635-21 to 21635-34 for affected products.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Legere Pharmaceuticals is recalling Rodex Forte dietary supplements because they contain undeclared food dyes. This could affect people with allergies to these dyes, though the recall doesn't mention specific health risks beyond potential allergic reactions.
The dietary supplement contains undeclared food dyes that could cause allergic reactions in sensitive individuals. The dyes are not listed on the product label, which may lead to unexpected allergic reactions in people with known sensitivities.
People who purchased Rodex Forte dietary supplements with batch codes 21635-21 to 21635-34 are affected. Those with allergies to Allura Red (Red No. 40) or Brilliant Blue (Blue No. 1) are at higher risk.
Check the batch code on the product label, which should be 21635-21, 21635-22, 21635-23, or 21635-34. The product is sold in 90-capsule bottles by Legere Pharmaceuticals.
Look for batch codes 21635-21 to 21635-34 on the label of the 90-capsule bottles.
The recall states the product contains undeclared dyes that could cause allergic reactions in sensitive individuals, but the official notice does not specify which allergies are affected.
Check the batch code on the label, which should be 21635-21, 21635-22, 21635-23, or 21635-34. The product is sold in 90-capsule bottles by Legere Pharmaceuticals.
The recall does not specify a remedy, so the official notice does not provide instructions for what to do with the product.
We’ve drafted a message you can send Legere Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0096-2025 — Legere Pharmaceuticals Legere Pharmaceuticals Hello, I own a Legere Pharmaceuticals that is covered by recall H-0096-2025 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.
