Garden of Life recalls certain joint supplements due to undeclared soy. Affected products include FYI ULTRA and ULTIMATE Joint & Cartilage Formula. Consumers should check lot numbers and expiration dates.
Undeclared Soy.
Garden of Life is recalling some joint supplements because they contain undeclared soy. This could be a problem for people with soy allergies or dietary restrictions. The affected products have specific lot numbers and expiration dates.
The supplements contain undeclared soy, which means they might cause allergic reactions or dietary issues for people sensitive to soy. This is a labeling issue rather than a safety hazard.
People who own or use the recalled joint supplements are affected. Those with soy allergies or dietary restrictions are at higher risk.
Check the product label for lot numbers 50312871, 50293: 50278965, or 5028258. The expiration dates range from October 2023 to June 2024.
Look for lot numbers 50312871, 50293093, 50278965, or 5028258 on the supplement packaging.
The hazard is undeclared soy, which could cause allergic reactions or dietary issues for people sensitive to soy.
The affected products are Garden of Life FYI ULTRA and ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement, 120 Ultra Zorbe capsules with specific lot numbers and expiration dates.
No, the recall is for undeclared soy, not a safety hazard. You can continue using the products if they are not the affected lot numbers.
We’ve drafted a message you can send Garden of Life to request your refund or repair — edit it as you like.
Subject: Recall F-0482-2024 — Garden of Life Garden of Life Hello, I own a Garden of Life that is covered by recall F-0482-2024 from Garden of Life. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.