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Use caution Food recall · FDA · Published March 17, 2017

Nutiva Plant Protein Shake Recall: Peanut Allergen Present

Nutiva recalls chocolate plant protein shakes due to detected peanut allergen at 4.7-4.8 ppm. Consumers should check product codes and contact Nutiva for details.

🇺🇸 FDA recall #F-1984-2017FoodNutiva ›
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Recalling firmNutiva213 W Cutting Blvd · Richmond, CA 94804-2015
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nutiva is recalling chocolate plant protein shakes because testing found peanut allergen at 4.7-4.8 ppm. This poses a risk for people with peanut allergies, as even small amounts can trigger reactions. Read more at govinfonow.com/recall/21993-nutiva-plant-protein-shake-recall-peanut-allergen-present.

Source Summary by GovInfoNow · govinfonow.com/recall/21993-nutiva-plant-protein-shake-recall-peanut-allergen-present · Updated October 8, 2026 · FDA enforcement record: FDA #F-1984-2017

Cite this page

“Nutiva Plant Protein Shake Recall: Peanut Allergen Present.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21993-nutiva-plant-protein-shake-recall-peanut-allergen-present. Based on FDA recall #F-1984-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1984-2017%22&limit=1).

Why it’s dangerous

The product contains peanut allergen at 4.7-4.8 ppm, which is above the safe threshold for people with severe peanut allergies. Even small amounts can cause allergic reactions in sensitive individuals.

Who’s affected

People with peanut allergies are at risk from this product. The recall affects Nutiva's chocolate plant protein shakes sold in the U.S. from May 2016 to November 2018.

How to tell if you have this one

Check for product codes: PBP101 (10-1.2 oz. packets) with UPCs 6-92752-10713-9 or 6-92752-10714-6, or PBP105 (21.6 oz. jars) with UPC 6-92752-10709-2. Products were sold from May 2016 to November 2018.

  • Brand
    Nutiva
  • Product
    Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Chocolate; Product # PBP101 - 10-1.2 oz. (34g)
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • 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.
Recall numberProduct, codes & lotsQuantity
F-1983-2017Nutiva 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; Product PBP201: Lot Code range: 06MAY2016-10NOV2016 Expiration Date Range: 06 MAY 2018 - 10 NOV 2018 Product PBP205: Lot Code Range: 03MAY2016 - 02MAR2017; Expiration Date Range: 03 MAY 2018 02 MAR 2019.PBP201 - 6,567 Units ; PBP205 - 31,438 units
F-1984-2017Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Chocolate; Product # PBP101 - 10-1.2 oz. (34g) packets ; Packet UPC/Caddy UPC: 6-92752-10713-9, 6-92752-10714-6; Master Case UPC: 6-92752-10715-3. Product # PBP105 - 21.6 oz. HDPE jar; Unit UPC: 6-92752-10709-2 Master Case UPC: 6-92752-10710-8; USDA Organic Certified, by Ecocert ICO; Product of the USA Vegan, Gluten Free, Non GMO. Manufactured for Nutiva, Richmond, CA 94804; Product PBP101: Lot Code range: 24MAY2016 11NOV2016 Expiration Date Range: 24 MAY 2018 11 NOV 2018 Product PBP105: Lot Code Range: 03MAY2016 11JAN2017; Expiration Date Range: 03 MAY 2018 11 JAN 2019PBP101 - 5,016 Units: PBP105 - 25,552 Units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Codes

    Look for UPCs 6-92752-10713-9, 6-92752-10714-6 for PBP101 packets or 6-92752-10709-2 for PBP105 jars.

Where it went and when

Where it was distributed

Distributed in 21 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: yesNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: yesKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA 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.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, California, Colorado, Connecticut, Florida, Georgia, Indiana, Iowa, Kansas, Kentucky, Nevada, New Hampshire, New Jersey, New York, North Carolina, Oregon, Pennsylvania, Texas, Virginia, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Mar 17, 201712. FDA classified it Class I: Apr 17, 201723. Published in FDA’s Enforcement Report: Apr 26, 201734. FDA terminated the recall: Nov 9, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1984-2017 (March 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1984-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA