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Lower risk Food recall · FDA · Published January 25, 2016

Nutrifruit Freeze Dried Black Raspberry Powder Recall: Label Error

Scenic Fruit Company recalls Nutrifruit Freeze Dried Black Raspberry Powder due to a label error listing 0g sugar instead of 2g per serving.

🇺🇸 FDA recall #F-0702-2016FoodNutrifruit ›
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Recalling firmScenic Fruit Company7510 Se Altman Rd · Gresham, OR 97080-8808
✎ GovInfoNow plain-language explainer

What happened, in plain English

Scenic Fruit Company is recalling Nutrifreeze Dried Black Raspberry Powder because the supplement facts panel incorrectly lists 0 grams of sugar per serving, when the correct amount is 2 grams. This affects items with UPC 0 79947 00019 0 sold in CA, KY, NC, ND, NV, PA, Canada, and online. The record does not specify a remedy or deadline for consumers. Read more at govinfonow.com/recall/25426-nutrifruit-freeze-dried-black-raspberry-powder-recall-label-error.

Source Summary by GovInfoNow · govinfonow.com/recall/25426-nutrifruit-freeze-dried-black-raspberry-powder-recall-label-error · Updated October 11, 2026 · FDA enforcement record: FDA #F-0702-2016

Cite this page

“Nutrifruit Freeze Dried Black Raspberry Powder Recall: Label Error.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/25426-nutrifruit-freeze-dried-black-raspberry-powder-recall-label-error. Based on FDA recall #F-0702-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0702-2016%22&limit=1).

Why it’s dangerous

The hazard is a labeling error where the supplement facts panel indicates 0 grams of sugar per serving instead of the correct 2 grams. This misleads consumers about the nutritional content of the product.

Who’s affected

Consumers who purchased Nutrifruit Freeze Dried Black Raspberry Powder (Item no. 30007 or 30041) in plastic jars from the listed states, Canada, or online. Individuals monitoring sugar intake may be affected by the inaccurate label information.

How to tell if you have this one

Check for Nutrifruit brand Freeze Dried Black Raspberry Powder in plastic jars with a net weight of 5 oz. Look for Item no. 30007 or 30041 and UPC 0 79947 00019 0. Verify the best-by date (e.g., 2/5/2016, 3/12/2016, etc.) or internal lot numbers such as D1417217, E0237054, or E1542303.

  • Brand
    Nutrifruit
  • Product
    Freeze Dried Black Raspberry Powder, Item no. 30007 or 30041. Nutrifruit brand. Each plastic jar has a net wt. 5 oz
  • 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 II
  • Status
    Terminated
  • Distribution
    distributed in CA, KY, NC, ND, NV, PA and Canada. The firm also sold product online.
Recall numberProduct, codes & lotsQuantity
F-0701-2016Freeze Dried Mango Powder, Item no. 30042. Nutrifruit brand. Each plastic jar has a net wt. 5 oz. The UPC is 0 79947 00110 4.; best by dates: 3/12/2016 8/2/2016 9/11/2016 4/13/2017 Lot code (internal): D1888255 E0140033 E0307070 E1486286331 units
F-0702-2016Freeze Dried Black Raspberry Powder, Item no. 30007 or 30041. Nutrifruit brand. Each plastic jar has a net wt. 5 oz. The UPC is 0 79947 00019 0.; Best by dates: 2/5/2016 3/12/2016 5/17/2016 8/23/2016 9/11/2016 10/23/2016 11/21/2016 1/21/2017 2/7/2017 2/27/2017 3/23/2017 4/13/2017 4/19/2017 4/30/2017 LOT NUMBERS (INTERNAL): Lot No. D1417217 D1902255 D2251321 E0237054 E0308070 E0595113 E0746141 E1148202 E1258219 E1347239 E1428266 E1482286 E1507292 E15423034813 units
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if you have Nutrifruit Freeze Dried Black Raspberry Powder with Item no. 30007 or 30041 and the specified UPC or lot numbers.

Where it went and when

Where it was distributed

Distributed in 6 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: yesNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “distributed in CA, KY, NC, ND, NV, PA and Canada. The firm also sold product online.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Kentucky, Nevada, North Carolina, North Dakota, Pennsylvania.

Recall timeline

FDA terminated this recall 16 months after the firm started it.

1. Firm started the recall: Jan 25, 201612. FDA classified it Class II: Feb 29, 201623. Published in FDA’s Enforcement Report: Mar 9, 201634. FDA terminated the recall: May 15, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class II
  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-0702-2016 (January 25, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0702-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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