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Astor Chocolate Corp. 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.

United States

TerminatedClass II

Company
Astor Chocolate Corp.
Product
Astor Chocolate Corporation Brand Dark Chocolate Covered Cra…
Recall date
October 31, 2017
Terminated
September 25, 2020
Source
FDA

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 Not published in this source record 1,149.6 lbs. of affected material was shipped through Astor Chocolate Corporations snack packaging program Dark Chocolate Covered Cranberries Supplier Lot Numbers: 17216, 29216, 31616, 01917, 13017, and 15817

Distribution

  • 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 sh

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0337-2018
Event ID
78436
Status
Terminated
Classification
Class II
Company
Astor Chocolate Corp.
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
Quantity
1,149.6 lbs. of affected material was shipped through Astor Chocolate Corporations snack packaging program
Reason
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.
Recall initiation date
October 31, 2017
Report date
November 29, 2017
Classification date
Not published in this source record
Termination date
September 25, 2020
Distribution pattern
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 sh
UPC, lot, and code information
Dark Chocolate Covered Cranberries Supplier Lot Numbers: 17216, 29216, 31616, 01917, 13017, and 15817
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Astor Chocolate Corp.

Other recalls from Astor Chocolate Corp.

FDA Recall United States Terminated Historical recordClass II

Astor Chocolate Corp.

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Published
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Distribution
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.