Recall record at a glance
| Official record | F-0337-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Astor Chocolate Corp. |
| Report date | Nov 29, 2017 |
| Recall initiation date | Oct 31, 2017 |
| Quantity | 1,149.6 lbs. of affected material was shipped through Astor Chocolate Corporations snack packaging program |
| Location | Lakewood, NJ, United States |
Official product 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
Why the product was recalled
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.
Distribution information
Distribution of 89 orders were within the United States across multiple states including the following: 1. New York 2. Florida 3. California 4. Wisconsin 5. Illinois 6. Colorado 7. Georgia 8. Oklahoma 9. Maryland 10. Ohio 11. Connecticut 12. New Jersey 13. Texas 14. Pennsylvania 15. North Carolina 16. Massachusetts 17. Minnesota 18. Tennessee 19. South Dakota 20. Idaho 21. South Carolina 22. Rhode Island Two orders were shipped to Quebec, Canada and two orders were shipped to Frigate Bay, Saint Kitts, Nevis.
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: E-Mail.
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.
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