Kiriko, LLC. recalls A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584,
FDA recalls A1 Slim dietary supplement due to undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine. This unapproved drug poses safety risks without established efficacy.
Recall notice
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
Contact the company & request your remedy
What happened, in plain English
The FDA has recalled A1 Slim dietary supplements because they contain undeclared drugs that haven't been approved for safety and effectiveness. This means the product could be harmful since it's not regulated as a safe supplement. Read more at govinfonow.com/recall/41157-a1-slim-dietary-supplement-recall-unapproved-drug-ingredients-found.
Source Summary by GovInfoNow · govinfonow.com/recall/41157-a1-slim-dietary-supplement-recall-unapproved-drug-ingredients-found · Updated October 7, 2026 · FDA enforcement record: FDA #D-0058-2018
Cite this page
“A1 Slim Dietary Supplement Recall: Unapproved Drug Ingredients Found.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41157-a1-slim-dietary-supplement-recall-unapproved-drug-ingredients-found. Based on FDA recall #D-0058-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0058-2018%22&limit=1).
Why it’s dangerous
The product contains undeclared drugs like sibutramine and phenolphthalein that haven't been approved by the FDA. These substances can cause health risks because they weren't tested for safety and effectiveness in the intended use.
Who’s affected
People who purchased A1 Slim dietary supplements from the manufacturer's website or retail stores. Those using the product for weight loss are most at risk due to potential health effects from unapproved ingredients.
How to tell if you have this one
Check for the product name 'A1 Slim', 350 mg capsules, 30-count bottles, and the bar code A105212014. The product was sold online at www.A1SLIM.COM and in stores with the manufacturer's address in Pearland, Texas.
- Brand
A1 Slim- Category
Drug
What to do — step by step
Check Product Details
Look for the product name 'A1 Slim', 350 mg capsules, 30-count bottles, and bar code A105212014 to confirm if you have the recalled item.
Questions people ask
Why was this product recalled?
The FDA found undeclared drugs like sibutramine and phenolphthalein in the product, which haven't been approved for safety and effectiveness.
What should I do if I have this product?
The recall record doesn't specify a remedy, so check the product details to see if it's affected and contact the manufacturer for guidance.
Is this product safe to use?
No, the product contains unapproved drugs that could pose health risks, so it's not safe to use.
Contact A1 Slim
We’ve drafted a message you can send A1 Slim to request your refund or repair — edit it as you like.
Subject: Recall D-0058-2018 — A1 Slim A1 Slim Hello, I own a A1 Slim that is covered by recall D-0058-2018 from A1 Slim. 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
Where this comes from
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.
- Official source: FDA Recall #D-0058-2018 (October 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0058-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
