Astor Chocolate Corporation Brand Dark Chocolate Covered Cranberries in Astor or Customer Logo packaging a. 1 oz. giveaway type package sizing b. 4 oz. giveaway type package sizing c. No best by date on units d. Individual cases sold to Astor branded customers i. Case counts include cases of: 1. 36 units 2. 50 units 3. 100 units 4. 150 units 5. 300 units
Class I - DangerousWhat Should You Do?
- Check if you have this product: Dark Chocolate Covered Cranberries Supplier Lot Numbers: 17216, 29216, 31616, 01917, 13017, and 15817
- 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:
- Astor Chocolate Corp.
- Reason for Recall:
- A supplier of Astor Chocolate Corporation has recalled an ingredient that the firm purchase and repackage as part of their snack packaging program due to undeclared MILK Allergen.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Astor Chocolate Corporation Brand Dark Chocolate Covered Cranberries in Astor or Customer Logo packaging a. 1 oz. giveaway type package sizing b. 4 oz. giveaway type package sizing c. No best by date on units d. Individual cases sold to Astor branded customers i. Case counts include cases of: 1. 36 units 2. 50 units 3. 100 units 4. 150 units 5. 300 units
Product Codes/Lot Numbers:
Dark Chocolate Covered Cranberries Supplier Lot Numbers: 17216, 29216, 31616, 01917, 13017, and 15817
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0337-2018
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