TruVision Health recalls Citrine Spark drink due to FDA-identified unsafe ingredients. Consumers should check lot numbers for affected products.
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruVision Health is recalling Citrine Spark drink because it contains ingredients (DMHA and hordenine) that the FDA says are unsafe for consumption. This recall affects consumers who bought the product with lot number PM17921F1.
The drink contains DMHA and hordenine, which the FDA has determined are not acceptable dietary ingredients. These substances may pose health risks when consumed, but the recall does not specify a mechanism for serious injury.
Anyone who purchased the TruBoost Drink Citrine Spark with lot number PM17921F1. The risk is low as the FDA has identified the ingredients as unsafe but no specific injury mechanism is described.
Check for the lot number PM17921F1 on the product label. The product is sold under the brand TruVision Health as TruBoost Drink Citrine Spark.
Look for the lot number PM17921F1 on the TruBoost Drink Citrine Spark label.
The FDA has determined that DMHA and hordenine are not acceptable dietary ingredients in this product.
Check the product label for lot number PM17921F1. If it matches, contact TruVision Health for further instructions.
The recall does not specify a mechanism for serious injury, so the risk is considered low.
We’ve drafted a message you can send TruVision Health to request your refund or repair — edit it as you like.
Subject: Recall F-0950-2023 — TruVision Health TruVision Health Hello, I own a TruVision Health that is covered by recall F-0950-2023 from TruVision Health. 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.