CLASS III Food recall · Reported 15 Jun 2022 · FDA Enforcement Report
Zydot Ultimate Blend The Original Detox Drink Natural recalled
Zydot Unlimited is recalling Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor. The recall was initiated on 6 May 2022 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1272-2022
- FDA event ID
- 90177
- Recalling firm
- Zydot Unlimited, Tulsa, OK
- Brand
- Zydot Ultimate
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 6 May 2022
- FDA classified
- 8 Jun 2022
- Reported
- 15 Jun 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Product category
- Other
Timeline
| 6 May 2022 | Recall initiated by company | |
| 8 Jun 2022 | Classified by FDA | +33 days |
| 15 Jun 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The ingredient list did not declare the preservatives (potassium sorbate, sodium benzoate) and food coloring (B1 and R40) in the product.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor 16 fl. oz. (473 ml) UPC packaged in plastic bottle with lid
Where it was distributed
USA
Questions about this recall
Is Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor recalled?
Yes. Zydot Unlimited recalled Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor on 6 May 2022. The recall is Class III and its status is Terminated. Recall number F-1272-2022.
Why was it recalled?
The ingredient list did not declare the preservatives (potassium sorbate, sodium benzoate) and food coloring (B1 and R40) in the product.
Which lots are affected?
Lot #s 092921LT, 031422LT
Where was it sold?
USA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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.
More recalls from Zydot Unlimited
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Zydot Ultimate Blend The Original Detox Drink Natural Orange Flavor recalledZydot Ultimate | Zydot Unlimited | Foreign Material | OK |
| Food | CLASS III | Zydot Ultimate Blend The Original Detox Drink Natural Cherry Flavor recalledZydot Ultimate | Zydot Unlimited | Foreign Material | OK |
| Food | CLASS II | Zydot Ultimate Blend Detox Drink Natural Tropical Ice Flavor recalledZydot Ultimate | Zydot Unlimited | Undeclared Allergens | OK |
Other Other recalls
All 4,664| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Alfalfa, Net Weight 50 lbs. bag, Product of USA, International recalledAlfalfa | International Sprout Holdings | Salmonella | 17 states |
| Food | CLASS I | Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalledCrown | Euro Foods Group USA NJ | Foreign Material | 4 states |
| Food | CLASS I | Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic recalledItem | Ron's Home Style Foods | Salmonella | AR, OK, TX |
| Food | CLASS I | Food to Live Organic SuperGrass Powder recalled by Lexunder | Lexunder | Salmonella | 40 states |
| Food | ANNOUNCED | Epinephrine Injection, USP 30 mg/ (1 mg/mL) multi dose vial recalledAmerican Regent, Inc. | American Regent | Particulate Matter | Nationwide |