CLASS I Drug recall · Reported 15 Aug 2018 · FDA Enforcement Report
Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot recalled
World Organix is recalling Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot, distributed nationwide in the US. The recall was initiated on 26 Jun 2018 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-1123-2018
- FDA event ID
- 80365
- Recalling firm
- World Organix, Las Vegas, NV
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 26 Jun 2018
- FDA classified
- 23 Aug 2018
- Reported
- 15 Aug 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Sterility
Timeline
| 26 Jun 2018 | Recall initiated by company | |
| 15 Aug 2018 | Published in enforcement report | +50 days |
| 23 Aug 2018 | Classified by FDA | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Blissful Remedies, 4 Hour Chill, Slow Motion Blend, Herbal Shot. 1.93 Fluid Oz (57ml) UPC#6 02401 88900 3.
Where it was distributed
Nationwide in the USA.
Questions about this recall
Why was it 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.
Which lots are affected?
Lot Code: 22. Best by date: 06/2019
Where was it sold?
Nationwide in the USA.
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
4 other products · FDA event 80365This product is part of a recall event; the main page for the event is Blissful Remedies Red Maeng Da recalled by World Organix.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Blissful Remedies Red Maeng Da recalled by World Organix | World Organix | Sterility | Nationwide | |
| CLASS I | Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa recalled | World Organix | Sterility | Nationwide | |
| CLASS I | Blissful Remedies Kratom+CBD infused Maeng Da, capsules recalled | World Organix | Sterility | Nationwide | |
| CLASS I | Blissful Remedies Gold Series Ultra Enhanced Indo recalled | World Organix | Sterility | Nationwide |
More recalls from World Organix
All 5| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Blissful Remedies Gold Series Ultra Enhanced Indo recalled | World Organix | Sterility | Nationwide |
| Drug | CLASS I | Blissful Remedies Kratom+CBD infused Maeng Da, capsules recalled | World Organix | Sterility | Nationwide |
| Drug | CLASS I | Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa recalled | World Organix | Sterility | Nationwide |
| Drug | CLASS I | Blissful Remedies Red Maeng Da recalled by World Organix | World Organix | Sterility | Nationwide |