Legere Pharmaceuticals recalls Super ProTHIN Plus dietary supplements containing undeclared Allura Red and Brilliant Blue dyes. Consumers should check product labels for the specific packet types and contact the company for details.
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Legere Pharmaceuticals is recalling Super ProTHIN Plus dietary supplements because they contain undeclared food dyes. This could pose risks for people with allergies to these dyes, though the recall does not mention specific injuries or illnesses.
The supplements contain undeclared food dyes that could cause allergic reactions in sensitive individuals. These dyes are not listed on the product label, which may lead to unintended consumption by people with known allergies.
People who purchased Super ProTHIN Plus dietary supplements from Legere Pharmaceuticals. Those with allergies to Allura Red (Red No. 40) or Brilliant Blue (Blue No. 1) are at higher risk.
Check for Super ProTHIN Plus dietary supplements in seven-packet sets (2 tablets and 4 capsules) or single packets with 14 Nutrilean capsules. The product does not have a UPC code.
Look for the specific packet types: seven packets with 2 tablets and 4 capsules, or one packet with 14 Nutrilean capsules.
The recall states the product contains undeclared dyes that could cause allergic reactions, so people with allergies to Allura Red or Brilliant Blue should avoid it.
Check for Super ProTHIN Plus in seven-packet sets (2 tablets and 4 capsules) or single packets with 14 Nutrilean capsules. The product does not have a UPC code.
The recall does not specify a remedy, so contact Legere Pharmaceuticals directly for guidance.
We’ve drafted a message you can send Legere Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0092-2025 — Legere Pharmaceuticals Legere Pharmaceuticals Hello, I own a Legere Pharmaceuticals that is covered by recall H-0092-2025 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.
