FDA recall record

Scenic Fruit Company Freeze Dried Black Raspberry Powder, Item no recall — FDA F-0702-2016

Label error in the supplement facts panel indicating 0 gram of sugar in each serving. The correct amount is 2 grams of sugar per serving.

Class IIclassification
F-0702-2016official record ID
Mar 9, 2016report date

Recall record at a glance

Official recordF-0702-2016
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmScenic Fruit Company
Report dateMar 9, 2016
Recall initiation dateJan 25, 2016
Quantity4813 units
LocationGresham, OR, United States

Official product description

Freeze 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.

Why the product was recalled

Label error in the supplement facts panel indicating 0 gram of sugar in each serving. The correct amount is 2 grams of sugar per serving.

Distribution information

distributed in CA, KY, NC, ND, NV, PA and Canada. The firm also sold product online.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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.

Related recall records

Other records from the same recalling company are shown first when available.