Ozona Organics LLC Recall: Products contain high water activity in the formula that provides a potential for microbial growth.
United States
TerminatedClass II
- Company
- Ozona Organics LLC
- Product
- OZONA ORGANICS LIQUID PROBIOTICS & GO HEALTHY LIQUID PROBIOT…
- Recall date
- July 14, 2023
- Terminated
- April 9, 2024
- Source
- FDA
Reason for recall
Products contain high water activity in the formula that provides a potential for microbial growth.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| OZONA ORGANICS LIQUID PROBIOTICS & GO HEALTHY LIQUID PROBIOTICS | Not published in this source record | 24,772 bottles | Lots #011122, 011228, 020810, 021115, 022023, 030115 and 030301. |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1616-2023
- Event ID
- 92715
- Status
- Terminated
- Classification
- Class II
- Company
- Ozona Organics LLC
- Product description
- OZONA ORGANICS LIQUID PROBIOTICS & GO HEALTHY LIQUID PROBIOTICS
- Quantity
- 24,772 bottles
- Reason
- Products contain high water activity in the formula that provides a potential for microbial growth.
- Recall initiation date
- July 14, 2023
- Report date
- October 4, 2023
- Classification date
- Not published in this source record
- Termination date
- April 9, 2024
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- Lots #011122, 011228, 020810, 021115, 022023, 030115 and 030301.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Ozona Organics LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
