VistaPharm recalls cherry-flavored activated charcoal drink (50g/240ml) that fails OTC monograph standards. Product may not meet safety requirements for over-the-counter use.
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
VistaPharm is recalling cherry-flavored activated charcoal drink (50g in 240ml) because it does not meet the required safety standards for over-the-counter use. This means the product might not be safe for consumers to use as intended.
The product failed to meet the official safety standards for over-the-counter medications. This means it might not be safe for consumption as intended, particularly for detox purposes.
People who purchased this specific activated charcoal drink from VistaPharm in the United States. Those using it for intended purposes like detoxification are most at risk.
Check for the product name 'KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR', 50 grams in 240 ml (8 fl oz), with lot number AE001 and expiration date 5/31/2026.
Look for the product name, size, lot number, and expiration date on the label.
The product does not meet the required safety standards for over-the-counter use, so it may not be safe.
The official recall notice does not specify a remedy, so you should check with VistaPharm for guidance.
Check for the product name 'KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR', 50 grams in 240 ml (8 fl oz), with lot number AE001 and expiration date 5/31/2026.
We’ve drafted a message you can send VistaPharm to request your refund or repair — edit it as you like.
Subject: Recall D-0590-2026 — VistaPharm VistaPharm Hello, I own a VistaPharm that is covered by recall D-0590-2026 from VistaPharm. 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.
