FDA Food recall · Reported April 26, 2017
Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets; Packet UPC/Caddy UPC: 6-92752-10716-0; 6-92752-10717-7; Master Case UPC: 6-92752-10718-4. Product # PBP205 - 21.6 oz. HDPE jar; Unit UPC: 6-92752-10711-5; Master Case UPC: 6-92752-10712-2 USDA Organic Certified, by Ecocert ICO; Product of the USA Vegan, Gluten Free, Non GMO. Manufactured for Nutiva, Richmond, CA 94804
Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testing found peanut allergen at 4.8 ppm.
Nutiva recalled Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # … - a critical-severity action.
Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # … was recalled by Nutiva in April 26, 2017. Reason: Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testi…. Check the official notice for the remedy. Verify recall #F-1983-2017 with the FDA Food before acting.
The recall
Nutiva issued this critical-severity FDA Food recall-Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testi….
- Critical
- severity level
- Class I
- classification
- April 26, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1983-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 5 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.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,014 dietary supplements recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Product description
Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets; Packet UPC/Caddy UPC: 6-92752-10716-0; 6-92752-10717-7; Master Case UPC: 6-92752-10718-4. Product # PBP205 - 21.6 oz. HDPE jar; Unit UPC: 6-92752-10711-5; Master Case UPC: 6-92752-10712-2 USDA Organic Certified, by Ecocert ICO; Product of the USA Vegan, Gluten Free, Non GMO. Manufactured for Nutiva, Richmond, CA 94804
Reason for recall
Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testing found peanut allergen at 4.8 ppm.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1983-2017 |
| Date reported | April 26, 2017 |
| Date initiated | March 17, 2017 |
| Recalling firm | Nutiva |
| Firm location | Richmond, CA |
| Affected scope | PBP201 - 6,567 Units ; PBP205 - 31,438 units |
| Distribution | Alabama, California, Colorado, Connecticut, Florida, Georgia, Indiana, Iowa, Kansas, Kentucky, Nevada, New Hampshire, New Jersey, New York, North Carolina, Oregon, Pennsylvania, Texas, Virginia, Washington, and Wisconsin. and to Hong Kong. |
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.
- Check the recall number (F-1983-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
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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Nationwide recalls with similar severity or category timing
Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Critical), closest by report date among other firms and states.
Similar Dietary Supplements · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026