CLASS I Drug recall · Reported 19 Jun 2019 · FDA Enforcement Report
Aphrodisiac Platinum 40000, Proprietary Raw Material recalled
Select Distributions is recalling Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg blister card, 24 cards per, distributed in Michigan, Ohio. The recall was initiated on 9 Apr 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-1344-2019
- FDA event ID
- 82594
- Recalling firm
- Select Distributions, Ferndale, MI
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 9 Apr 2019
- FDA classified
- 13 Jun 2019
- Reported
- 19 Jun 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Hidden Drug Ingredients
Timeline
| 9 Apr 2019 | Recall initiated by company | |
| 13 Jun 2019 | Classified by FDA | +65 days |
| 19 Jun 2019 | 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 has found the product to be tainted with sildenafil
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: APhrodisiac. UPC Code 644118128135
Where it was distributed
MI, OH
Questions about this recall
Is Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg blister card, 24 cards per recalled?
Yes. Select Distributions recalled Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg blister card, 24 cards per on 9 Apr 2019. The recall is Class I and its status is Terminated. Recall number D-1344-2019.
Why was it recalled?
Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil
Which lots are affected?
All lots
Where was it sold?
MI, OH
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.