CLASS I Drug recall · Reported 25 Dec 2013 · FDA Enforcement Report
72HP Maximum Potency Male Sexual Enhancement recalled
Fabscout Entertainment is recalling 72HP Maximum Potency Male Sexual Enhancement, Dietary Supplement, supplied in per, distributed in California, Florida, Utah. The recall was initiated on 14 Aug 2013 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-377-2014
- FDA event ID
- 66043
- Recalling firm
- Fabscout Entertainment, Ft Lauderdale, FL
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 14 Aug 2013
- FDA classified
- 18 Dec 2013
- Reported
- 25 Dec 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Labeling Errors
Timeline
| 14 Aug 2013 | Recall initiated by company | |
| 18 Dec 2013 | Classified by FDA | +126 days |
| 25 Dec 2013 | Published in enforcement report | +7 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 were found to contain undeclared sildenafil
Product as listed by the FDA
72HP MAXIMUM POTENCY MALE SEXUAL ENHANCEMENT, Dietary Supplement, supplied in 1 capsule per blister pack, Distributed by: 72HP, Inc. Weston, FL
Where it was distributed
CA, FL and UT
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA: products were found to contain undeclared sildenafil
Which lots are affected?
All Lots
Where was it sold?
CA, FL and UT
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 66043| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Pro Power Max Natural Energy Enhancer, All Natural Herbs recalled | Fabscout Entertainment | Labeling Errors | CA, FL, UT | |
| CLASS I | Evil Root 1200 mg, supplied in per, Manufacturer recalled | Fabscout Entertainment | Labeling Errors | CA, FL, UT |
More recalls from Fabscout Entertainment
All 5| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Clalis capsules, 50 mg bottle ( labeling is in foreign language) recalled | Fabscout Entertainment | Labeling Errors | Nationwide |
| Drug | CLASS I | Silver Sword capsules, 180 mg clamshell tin recalled | Fabscout Entertainment | Labeling Errors | Nationwide |
| Drug | CLASS I | Evil Root 1200 mg, supplied in per, Manufacturer recalled | Fabscout Entertainment | Labeling Errors | CA, FL, UT |
| Drug | CLASS I | Pro Power Max Natural Energy Enhancer, All Natural Herbs recalled | Fabscout Entertainment | Labeling Errors | CA, FL, UT |