Why it was recalled
Marketed Without An Approved NDA/ANDA
Product description
Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.
Lot numbers, UPCs & expiration codes
Lot 2108; EXP 10/31/2024
Where it was sold
Distribution worldwide via amazon.com
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-0494-2024
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Apr 22, 2024
- FDA report date
- May 22, 2024
- Quantity
- 5 boxes
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Stop Clopez Corp
Original FDA data
Every field from FDA enforcement report D-0494-2024, exactly as published.
Show all FDA fields
- City
- Miramar
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 94455
- Address
- 2301 Island Dr
- Code information
- Lot 2108; EXP 10/31/2024
- Postal code
- 33023-3546
- Report date
- May 22, 2024
- Product type
- Drugs
- Recall number
- D-0494-2024
- Classification
- Class I
- Recalling firm
- Stop Clopez Corp
- Product quantity
- 5 boxes
- Termination date
- Apr 8, 2025
- Reason for recall
- Marketed Without An Approved NDA/ANDA
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.
- Distribution pattern
- Distribution worldwide via amazon.com
- Recall initiation date
- Apr 22, 2024
- Center classification date
- May 13, 2024