CLASS I ONGOING Drug recall · Reported 1 May 2024 · FDA Enforcement Report
libigrow RED Dragon+, Maximum Strength Formula recalled
Pyramids Wholesale is recalling libigrow RED Dragon+, Maximum Strength Formula per, distributed nationwide in the US. The recall was initiated on 19 Mar 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-0454-2024
- FDA event ID
- 94265
- Recalling firm
- Pyramids Wholesale, Los Angeles, CA
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 19 Mar 2024
- FDA classified
- 22 Apr 2024
- Reported
- 1 May 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 19 Mar 2024 | Recall initiated by company | |
| 22 Apr 2024 | Classified by FDA | +34 days |
| 1 May 2024 | Published in enforcement report | +9 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: Products found to contain undeclared sildenafil and/or tadalafil.
Product as listed by the FDA
libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.
Where it was distributed
Nationwide in the USA
Questions about this recall
Is libigrow RED Dragon+, Maximum Strength Formula per recalled?
Yes. Pyramids Wholesale recalled libigrow RED Dragon+, Maximum Strength Formula per on 19 Mar 2024. The recall is Class I and its status is Ongoing. Recall number D-0454-2024.
Why was it recalled?
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Which lots are affected?
All lots
Where was it sold?
Nationwide in the USA
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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