Chocolate Dipped Almond Biscotti, in various sizes, wrapped in plastic, with "Enjoy By" dates prior to 091614, manufactured by Semifreddi's Inc, Alameda, CA. Product Size and UPC codes: 0.65 oz., case of 100 units 758843915943 0.89 oz., tub of 22 units 758843916001 1.3 oz., box of 4 units 758843915745 1.3 oz., box of 12 units 758843915967 1.3 oz., case of 50 units 758843915905
Class I - DangerousWhat Should You Do?
- Check if you have this product: with Enjoy By date prior to 091614
- 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:
- Semifreddi's Inc.
- Reason for Recall:
- Semifreddi's Almond Biscotti and Semifreddi's Chocolate Dipped Almond Biscotti are being recalled due to undeclared allergens, milk and soy; butter did not list milk as a subingredient; lecithin did not list soy as a subingredient.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Chocolate Dipped Almond Biscotti, in various sizes, wrapped in plastic, with "Enjoy By" dates prior to 091614, manufactured by Semifreddi's Inc, Alameda, CA. Product Size and UPC codes: 0.65 oz., case of 100 units 758843915943 0.89 oz., tub of 22 units 758843916001 1.3 oz., box of 4 units 758843915745 1.3 oz., box of 12 units 758843915967 1.3 oz., case of 50 units 758843915905
Product Codes/Lot Numbers:
with Enjoy By date prior to 091614
Distribution:
Distributed in: AZ, CO, NE, NJ, NY, OR, WA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1948-2013
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