Severity
Moderate
FDA Food recall · Reported December 11, 2024
After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
Dyma Brands recalled REJUV ORIGINALS LOW CALORIE ORANGE DRINK MIX NATURAL FLAVOR, NET WT. 8.6 OZ. (244g), UPC … - a moderate-severity action.
REJUV ORIGINALS LOW CALORIE ORANGE DRINK MIX NATURAL FLAVOR, NET WT. 8.6 OZ. (244g), UPC … was recalled by Dyma Brands in December 11, 2024. Reason: After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each pro…. Check the official notice for the remedy. Verify recall #F-0228-2025 with the FDA Food before acting.
The recall
Dyma Brands issued this moderate-severity FDA Food recall-After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each pro….
Sourced from official FDA Food enforcement records. Verify recall #F-0228-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0228-2025) was formally reported on December 11, 2024, with the manufacturer initiating the action on October 2, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Dyma Brands is listed as the recalling firm, operating out of Atlanta, GA. Federal records list the affected scope as 11cs/12/806oz pouch.
The documented reason for this recall is: After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products. Distribution data in the federal record shows the product reached: Products were distributed to the following states: AR, AZ, CA, CO, CT, FL, GA, IA, IL, LA, MD, MI, MN, MO, NC, ND, NE, NJ, NM, NV, OH, OK, OR, PA, TN, TX, UT, WA, WI & WV.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
11cs/12/806oz pouch
Related Recalls
6
2 from same agency
REJUV ORIGINALS LOW CALORIE ORANGE DRINK MIX NATURAL FLAVOR, NET WT. 8.6 OZ. (244g), UPC 8 22486 14388 6, Case UPC 30822486143887, MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTON, TX 77043
After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | F-0228-2025 |
| Date reported | December 11, 2024 |
| Date initiated | October 2, 2024 |
| Recalling firm | Dyma Brands |
| Firm location | Atlanta, GA |
| Affected scope | 11cs/12/806oz pouch |
| Distribution | Products were distributed to the following states: AR, AZ, CA, CO, CT, FL, GA, IA, IL, LA, MD, MI, MN, MO, NC, ND, NE, NJ, NM, NV, OH, OK, OR, PA, TN, TX, UT, WA, WI & WV. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 11, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.