Legere Pharmaceuticals recalls 90-count Probese Caps dietary supplements with iron due to undeclared Allura Red and Brilliant Blue dyes. Consumers should check product codes for affected batches.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Legere Pharmaceuticals is recalling 90-count Probese Caps iron supplements because they contain undeclared food dyes. This recall is important because the dyes were not listed on the product label, which could lead to allergic reactions or other health issues for sensitive individuals.
The capsules contain undeclared food dyes that may cause allergic reactions in sensitive individuals. These dyes are not listed on the product label, which is required by food safety regulations.
People who own or use the recalled Probese Caps dietary supplements with iron. Those with allergies to Allura Red (Red No. 40) or Brilliant Blue (Blue No. 1) are at higher risk.
Check for 90-count bottles labeled 'Probese Caps' with iron. The product codes include 21874-19 through 21874-25. The manufacturer address is 15344 N 83rd way, Scottsdale AZ 85260.
Look for the product codes 21874-19 through 21874-25 on the bottle.
The capsules contain undeclared food dyes (Allura Red and Brilliant Blue) that were not listed on the product label.
Check the product codes to see if it's affected. If it is, contact Legere Pharmaceuticals for instructions.
Yes, individuals with allergies to Allura Red (Red No. 40) or Brilliant Blue (Blue No. 1) may experience allergic reactions.
We’ve drafted a message you can send Legere Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0094-2025 — Legere Pharmaceuticals Legere Pharmaceuticals Hello, I own a Legere Pharmaceuticals that is covered by recall H-0094-2025 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.
