Severity
Low
The recall
Vita 360, LLC issued this low-severity FDA Food recall — FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 1….
Sourced from official FDA Food enforcement records. Verify recall #F-0710-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0710-2024) was formally reported on January 17, 2024, with the manufacturer initiating the action on December 7, 2023. It is classified under Low severity (Class III), with a current status of Terminated. Vita 360, LLC is listed as the recalling firm, operating out of San Juan, PR. Federal records indicate 1999 units units are affected.
The documented reason for this recall is: FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared. Distribution data in the federal record shows the product reached: Domestic distribution only throughout Puerto Rico. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Food. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 2 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified low severity.
Severity
Low
Units Affected
1999 units
Related Recalls
6
6 from same agency
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
FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0710-2024 |
| Date reported | January 17, 2024 |
| Date initiated | December 7, 2023 |
| Recalling firm | Vita 360, LLC |
| Units affected | 1999 units |
| Distribution | Domestic distribution only throughout Puerto Rico |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported January 17, 2024.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).