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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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 E1542303
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Scenic Fruit Company
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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.
Product Codes/Lot Numbers:
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 E1542303
Distribution:
Distributed in: CA, KY, NC, ND, NV, PA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0702-2016
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