His Enterprise Miss Slim Capsules Recall: Unapproved Drug Product
His Enterprise recalls Miss Slim capsules (10-count and 30-count boxes) due to being marketed without FDA approval. Consumers should check UPC 742137605030 for affected products.
Recall notice
Marketed without ANDA/NDA approval
Contact the company
What happened, in plain English
His Enterprise is recalling Miss Slim capsules because they were sold without proper FDA approval. This means the product may not be safe or effective, and consumers should stop using it. Read more at govinfonow.com/recall/36068-his-enterprise-miss-slim-capsules-recall-unapproved-drug-product.
Source Summary by GovInfoNow · govinfonow.com/recall/36068-his-enterprise-miss-slim-capsules-recall-unapproved-drug-product · Updated August 18, 2026 · FDA enforcement record: FDA #D-0770-2021
Cite this page
“His Enterprise Miss Slim Capsules Recall: Unapproved Drug Product.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/36068-his-enterprise-miss-slim-capsules-recall-unapproved-drug-product. Based on FDA recall #D-0770-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0770-2021%22&limit=1).
Why it’s dangerous
The product was marketed without FDA approval, which means it hasn't been tested for safety or effectiveness. This could lead to health risks if used without proper oversight.
Who’s affected
Anyone who owns or uses Miss Slim capsules from His Enterprise. People who have the product are most at risk due to the unapproved status.
How to tell if you have this one
Check for Miss Slim capsules in 10-count or 30-count boxes with UPC 742137605030. All lots of this product are affected.
- Brand
His Enterprise- Product
Miss Slim, capsules, packaged in 10-count and 30-count box, Distributed by : His Enterprise Made in USA UPC 742137605030- Category
Drug
What to do — step by step
Check Product Details
Look for the UPC code 742137605030 on the box to confirm if you have the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “USA nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 43 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-0770-2021 (July 20, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0770-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 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.