Recall record at a glance
| Official record | F-1983-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Nutiva |
| Report date | Apr 26, 2017 |
| Recall initiation date | Mar 17, 2017 |
| Quantity | PBP201 - 6,567 Units ; PBP205 - 31,438 units |
| Location | Richmond, CA, United States |
Official 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
Why the product was recalled
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.
Distribution information
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.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.