Legere Pharmaceuticals recalls Protrim Plus dietary supplements due to undeclared Allura Red and Brilliant Blue dyes in gelatin capsules. Consumers should check product labels for the specific batch.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Legere Pharmaceuticals is recalling Protrim Plus dietary supplements because they contain undeclared food dyes (Allura Red and Brilliant Blue) in the gelatin capsules. This could pose a risk for people with allergies to these dyes, though the recall does not specify a risk of serious injury.
The dietary supplement contains undeclared food dyes that could cause allergic reactions in sensitive individuals. The dyes are listed as Allura Red (Red No. 40) and Brilliant Blue (Blue No. 1) in the gelatin capsules.
People who have purchased Protrim Plus dietary supplements from Legere Pharmaceuticals are likely affected. Those with allergies to Allura Red (Red No. 40) or Brilliant Blue (Blue No. 1) are at higher risk.
Check for the product name 'Protrim Plus' on the label. The product was sold by Legere Pharmaceuticals in Scottsdale, AZ, with a specific product code (21634-9).
Look for the product name 'Protrim Plus' and the specific product code (21634-9) on the label.
The recall does not state that the product is unsafe for general use; it is recalled due to undeclared dyes that may cause allergic reactions in sensitive individuals.
The recall record does not specify a remedy, so there is no action required beyond checking the product label.
The recall mentions that the dyes could cause allergic reactions in people sensitive to Allura Red (Red No. 40) or Brilliant Blue (Blue No. 1).
We’ve drafted a message you can send Legere Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0093-2025 — Legere Pharmaceuticals Legere Pharmaceuticals Hello, I own a Legere Pharmaceuticals that is covered by recall H-0093-2025 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.
