CLASS I Drug recall · Reported 5 Jun 2019 · FDA Enforcement Report
The Beast, The Beast can be taken under the situation recalled
Stiff Boy is recalling The Beast, The Beast can be taken under the situation of Heart disease and even after, distributed nationwide in the US. The recall was initiated on 6 May 2019 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-1321-2019
- FDA event ID
- 82704
- Recalling firm
- Stiff Boy, Englewood, NJ
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 6 May 2019
- FDA classified
- 5 Jun 2019
- Reported
- 5 Jun 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 6 May 2019 | Recall initiated by company | |
| 5 Jun 2019 | Classified by FDA | +30 days |
| 5 Jun 2019 | Published in enforcement report | +0 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: The Beast contains undeclared sildenafil which was discovered through FDA analysis.
Product as listed by the FDA
The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules per packet.
Where it was distributed
Nationwide
Questions about this recall
Is The Beast, The Beast can be taken under the situation of Heart disease and even after recalled?
Yes. Stiff Boy recalled The Beast, The Beast can be taken under the situation of Heart disease and even after on 6 May 2019. The recall is Class I and its status is Terminated. Recall number D-1321-2019.
Why was it recalled?
Marketed without an Approved NDA/ANDA: The Beast contains undeclared sildenafil which was discovered through FDA analysis.
Which lots are affected?
All lots
Where was it sold?
Nationwide
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.