CLASS I ONGOING Drug recall · Reported 28 Feb 2024 · FDA Enforcement Report
Schwinnng Herbal Dietary Supplement recalled by Today The World
Today The World is recalling Schwinnng Herbal Dietary Supplement, distributed nationwide in the US. The recall was initiated on 6 Feb 2024 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0344-2024
- FDA event ID
- 93941
- Recalling firm
- Today The World, Portland, OR
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 6 Feb 2024
- FDA classified
- 22 Feb 2024
- Reported
- 28 Feb 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 6 Feb 2024 | Recall initiated by company | |
| 22 Feb 2024 | Classified by FDA | +16 days |
| 28 Feb 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.
Product as listed by the FDA
SCHWINNNG Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Today the World LLC, Vancouver, WA 98683
Where it was distributed
Product distributed nationwide within the United States.
Questions about this recall
Why was it recalled?
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.
Which lots are affected?
Lot #: 2108, Exp. Date 10/31/2024.
Where was it sold?
Product distributed nationwide within the United States.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
2 other products · FDA event 93941This product is part of a recall event; the main page for the event is Arize Herbal Dietary Supplement recalled by Today The World.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Arize Herbal Dietary Supplement recalled by Today The World | Today The World | Labeling Errors | Nationwide | |
| CLASS I | Sustain Herbal Dietary Supplement recalled by Today The World | Today The World | Labeling Errors | Nationwide |
More recalls from Today The World
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Sustain Herbal Dietary Supplement recalled by Today The World | Today The World | Labeling Errors | Nationwide |
| Drug | CLASS I | Arize Herbal Dietary Supplement recalled by Today The World | Today The World | Labeling Errors | Nationwide |