Vita 360, LLC Recall: FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
United States
TerminatedClass III
- Company
- Vita 360, LLC
- Product
- Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb…
- Recall date
- December 7, 2023
- Terminated
- May 1, 2024
- Source
- FDA
Reason for recall
FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle. Container description: White Plastic Bottle 300CC with white cap sealed with clear plastic Total Package size: Master Case with 81 Bottles containing 120 capsules each one. Lot no. 2633, Exp. 07/25 Manufactured in the US | Not published in this source record | 1999 units | Manufacturer Lot #2633; Expiration Date: 07/25 |
Distribution
- Domestic distribution only throughout Puerto Rico
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0710-2024
- Event ID
- 93627
- Status
- Terminated
- Classification
- Class III
- Company
- Vita 360, LLC
- Product description
- Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle. Container description: White Plastic Bottle 300CC with white cap sealed with clear plastic Total Package size: Master Case with 81 Bottles containing 120 capsules each one. Lot no. 2633, Exp. 07/25 Manufactured in the US
- Quantity
- 1999 units
- Reason
- FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
- Recall initiation date
- December 7, 2023
- Report date
- January 17, 2024
- Classification date
- Not published in this source record
- Termination date
- May 1, 2024
- Distribution pattern
- Domestic distribution only throughout Puerto Rico
- UPC, lot, and code information
- Manufacturer Lot #2633; Expiration Date: 07/25
- 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: Vita 360, LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
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 III mean?
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
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.
