Stop using nowDrug recall · FDA · Published August 27, 2015
Recall: Miracle Diet 30 Capsules Due to Undeclared Phenolphthalein
The One Minute Miracle Inc recalls Miracle Diet 30 capsules because they contain undeclared phenolphthalein, a drug removed from the market for safety reasons.
Marketed Without An Approved NDA/ANDA: Miracle Diet 30 was found to contain undeclared phenolphthalein, a drug product once contained in over-the-counter laxatives but was taken off the U.S. market due to safety concerns, making this product an unapproved drug.
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Contact the company
📍Recalling firmThe One Minute Miracle Inc3322 NE 166th St · North Miami Beach, FL 33160-3844
✎ GovInfoNow plain-language explainer
The One Minute Miracle Inc is recalling Miracle Diet 30 capsules because the product contains undeclared phenolphthalein. Phenolphthalein was previously used in over-the-counter laxatives but was removed from the U.S. market due to safety concerns. Because of this ingredient, the product is considered an unapproved drug. Read more at govinfonow.com/recall/43783-the-one-minute-miracle-inc-recalls-miracle-diet-30-capsules.
“Recall: Miracle Diet 30 Capsules Due to Undeclared Phenolphthalein.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/43783-the-one-minute-miracle-inc-recalls-miracle-diet-30-capsules. Based on FDA recall #D-0230-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0230-2016%22&limit=1).
The Food and Drug Administration announced on Aug. 27, 2015, that The One Minute Miracle Inc. is recalling Miracle Diet 30 capsules because they contain undeclared phenolphthalein, an unapproved drug ingredient. Consumers should stop using the product immediately.
How to tell if you have it
Brand: The One Minute Miracle Inc
Product: Miracle Diet 30 Capsules
UPC: 7 538073516768
Expiration Date: through 04/15/2018
The hazard
The product contains undeclared phenolphthalein, a drug once used in over-the-counter laxatives but removed from the U.S. market due to safety concerns. This makes Miracle Diet 30 an unapproved drug.
Context
GovInfoNow's records show other recent recalls of similar products include Buy-Herbal Kian Pee Wan Capsules (2026-03-21) and StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15). Xyvona (Levorphanol) 2mg Tablet Recall was also reported on 2026-05-22.
How to tell if you have this one
Check your bottle for the brand name 'Miracle Diet 30' and the manufacturer 'The One Minute Miracle Inc.' Look for UPC 7 538073516768 and verify the expiration date is on or before 04/15/2018.
Brand
The One Minute Miracle Inc
Product
MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7
Category
Drug
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
Nationwide
Recall number
Product, codes & lots
Quantity
D-0229-2016
MIRACLE ROCK 48 capsules, packaged in 2 x 2-count blisters, 4-count capsules per carton, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 0911312397354.; All lots through Expiration Date 06/01/2018
688 cartons
D-0230-2016
MIRACLE DIET 30 capsules, 30-count bottle, Manufactured Exclusively For: The One Minute Miracle Inc., UPC 7 538073516768.; All lots through Expiration Date 04/15/2018
1 bottle
Based on the official FDA remedy
What to do — step by step
Stop Using the Product
Do not consume the Miracle Diet 30 capsules if you have them.
Check Expiration Date
Verify that your bottle's expiration date is through 04/15/2018 to confirm it is part of the recall.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “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 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-0230-2016 (August 27, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0230-2016 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 12, 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.