Why it was recalled
Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.
Product description
Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot. 1.93 Fluid Oz (57ml) UPC#6 02401 88900 3.
Lot numbers, UPCs & expiration codes
Lot Code: 22. Best by date: 06/2019
Where it was sold
Nationwide in the USA.
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-1123-2018
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Jun 26, 2018
- FDA report date
- Aug 15, 2018
- Quantity
- 164 2oz bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- World Organix, LLC
Original FDA data
Every field from FDA enforcement report D-1123-2018, exactly as published.
Show all FDA fields
- City
- Las Vegas
- State
- NV
- Status
- Terminated
- Country
- United States
- Event ID
- 80365
- Address
- 6149 S. Rainbow Blvd #5
- Code information
- Lot Code: 22. Best by date: 06/2019
- Postal code
- 89118
- Report date
- Aug 15, 2018
- Product type
- Drugs
- Recall number
- D-1123-2018
- Classification
- Class I
- Recalling firm
- World Organix, LLC
- Product quantity
- 164 2oz bottles
- Termination date
- Sep 30, 2024
- Reason for recall
- Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot. 1.93 Fluid Oz (57ml) UPC#6 02401 88900 3.
- Distribution pattern
- Nationwide in the USA.
- Recall initiation date
- Jun 26, 2018
- Center classification date
- Aug 23, 2018