Severity
Critical
FDA Food recall · Reported March 13, 2013
Herbalife of America Inc is initiating this recall due to trace amounts of an undeclared milk protein allergen.
Herbalife International Of America Inc recalled HERBALIFE Formula 1 Instant Healthy Meal, Nutritional Shake Mix ( Vanilla Dream) Packets;… - a critical-severity action.
HERBALIFE Formula 1 Instant Healthy Meal, Nutritional Shake Mix ( Vanilla Dream) Packets;… was recalled by Herbalife International Of America Inc in March 13, 2013. Reason: Herbalife of America Inc is initiating this recall due to trace amounts of an undeclared milk protein allerge…. Check the official notice for the remedy. Verify recall #F-1059-2013 with the FDA Food before acting.
The recall
Herbalife International Of America Inc issued this critical-severity FDA Food recall-Herbalife of America Inc is initiating this recall due to trace amounts of an undeclared milk protein allerge….
Sourced from official FDA Food enforcement records. Verify recall #F-1059-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1059-2013) was formally reported on March 13, 2013, with the manufacturer initiating the action on February 20, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Herbalife International Of America Inc is listed as the recalling firm, operating out of Torrance, CA. Federal records list the affected scope as 5,928 (2,732 cartons and3,196 IBP Kits).
The documented reason for this recall is: Herbalife of America Inc is initiating this recall due to trace amounts of an undeclared milk protein allergen. Distribution data in the federal record shows the product reached: Worldwide distribution.. 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, 6 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 - 2,002 dietary supplements 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
5,928 (2,732 cartons and3,196 IBP Kits)
Related Recalls
6
6 from same agency
HERBALIFE Formula 1 Instant Healthy Meal, Nutritional Shake Mix ( Vanilla Dream) Packets; net WT 1.83 oz/52 g; packaged as 12 packets in a cardboard carton; just add water; single serve powder in a packet;
Herbalife of America Inc is initiating this recall due to trace amounts of an undeclared milk protein allergen.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1059-2013 |
| Date reported | March 13, 2013 |
| Date initiated | February 20, 2013 |
| Recalling firm | Herbalife International Of America Inc |
| Firm location | Torrance, CA |
| Affected scope | 5,928 (2,732 cartons and3,196 IBP Kits) |
| Distribution | Worldwide distribution. |
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 March 13, 2013. 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.