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Class I: serious health riskTerminated

Select Distributions Aphrodisiac Platinum 40000 Recall

Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24…

SELECT DISTRIBUTIONS LLC · Ferndale, MI

Risk level
Class I
Reported by FDA
Jun 19, 2019
Recall ID
D-1344-2019
Check your lot numberHow we source this data

Summary

Select Distributions recalled Aphrodisiac Platinum 40000 starting Apr 9, 2019. The FDA classified it as Class I (serious health risk) and published enforcement report D-1344-2019 on Jun 19, 2019. Reason: Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil. Status: Terminated.

Why it was recalled

Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil

Product description

Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: APhrodisiac. UPC Code 644118128135

Lot numbers, UPCs & expiration codes

All lots

Where it was sold

MI, OH

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1344-2019
Classification
Class I
Status
Terminated
Recall initiated
Apr 9, 2019
FDA report date
Jun 19, 2019
Quantity
60 boxes
Recall type
Voluntary: Firm initiated
Recalling firm
SELECT DISTRIBUTIONS LLC

Original FDA data

Every field from FDA enforcement report D-1344-2019, exactly as published.

Show all FDA fields
City
Ferndale
State
MI
Status
Terminated
Country
United States
Event ID
82594
Address
1320 W 9 Mile Rd
Code information
All lots
Postal code
48220
Report date
Jun 19, 2019
Product type
Drugs
Recall number
D-1344-2019
Classification
Class I
Recalling firm
SELECT DISTRIBUTIONS LLC
Product quantity
60 boxes
Termination date
Oct 16, 2023
Reason for recall
Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil
Voluntary / mandated
Voluntary: Firm initiated
Product description
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: APhrodisiac. UPC Code 644118128135
Distribution pattern
MI, OH
Recall initiation date
Apr 9, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Jun 13, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1344-2019, published Jun 19, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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