Food, drugs, devices › Gilster-Mary Lee Corp.
Food recall: Food Lion Creamy Chocolate Frosting, Net Wt 16 OZ, Distributed by Food Lion, LLC, Salisbury, NC, foodlion.com, packaged
FDA enforcement event 84064 is a food recall by Gilster-Mary Lee Corp. of Chester, IL, initiated 16 Oct 2019 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 56% of the 516 food enforcement events initiated in 2019 carry the same class.
Status: Terminated, terminated 4 Dec 2019. Initiation: voluntary: firm initiated. Gilster-Mary Lee Corp. has 11 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Gilster-Mary Lee Corp., Chester, IL.
Reason for recall
"Cream cheese frosting was put in a container labeled as Creamy Chocolate Frosting. The chocolate frosting label fails to declare the presence of the major food allergen Milk."
Distribution
"Shipped to one customer in North Carolina"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0149-2020 | Food Lion Creamy Chocolate Frosting, Net Wt 16 OZ, Distributed by Food Lion, LLC, Salisbury, NC, foodlion.com, packaged in 12 cans per case. | 66 cases | Class II | Terminated | 20 Nov 2019 |
Context
Other enforcement events for Gilster-Mary Lee Corp.
All 11 events for Gilster-Mary Lee Corp.
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Cream cheese frosting was put in a container labeled as Creamy Chocolate Frosting. The chocolate frosting label fails to declare the presence of the major food allergen Milk."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Shipped to one customer in North Carolina"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 4 Dec 2019. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.