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Class I: serious health riskTerminated

Nutiva Nuture Vitality Organic Plant Protein Recall

Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla

Nutiva · Richmond, CA

Risk level
Class I
Reported by FDA
Apr 26, 2017
Recall ID
F-1983-2017
Check your lot numberHow we source this data

Summary

Nutiva recalled Nutiva Nuture Vitality Organic Plant Protein starting Mar 17, 2017. The FDA classified it as Class I (serious health risk) and published enforcement report F-1983-2017 on Apr 26, 2017. Reason: 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. Status: Terminated.

Why it 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.

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

Lot numbers, UPCs & expiration codes

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.

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1983-2017
Classification
Class I
Status
Terminated
Recall initiated
Mar 17, 2017
FDA report date
Apr 26, 2017
Quantity
PBP201 - 6,567 Units ; PBP205 - 31,438 units
Recall type
Voluntary: Firm initiated
Recalling firm
Nutiva

Original FDA data

Every field from FDA enforcement report F-1983-2017, exactly as published.

Show all FDA fields
City
Richmond
State
CA
Status
Terminated
Country
United States
Event ID
76773
Address
213 W Cutting Blvd
Code information
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.
Postal code
94804-2015
Report date
Apr 26, 2017
Product type
Food
Recall number
F-1983-2017
Classification
Class I
Recalling firm
Nutiva
Product quantity
PBP201 - 6,567 Units ; PBP205 - 31,438 units
Termination date
Nov 9, 2017
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.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
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 initiation date
Mar 17, 2017
Initial firm notification
Press Release
Center classification date
Apr 17, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1983-2017, published Apr 26, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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