Food, drugs, devices › Gilster-Mary Lee Corp.
Food recall: Food Club Chocolate Chunk Brownie Mix, packaged in 21.5-oz. boxes, UPC# 36800-13486, distributed by TOPCO Associates LLC
Gilster-Mary Lee Corp. (Chester, IL) initiated this food recall on 2 Jan 2013; FDA lists 1 product record under event 64009, classified Class I.
FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 37% of the 546 food enforcement events initiated in 2013 carry the same class.
Status: Terminated, terminated 13 Feb 2014. 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
"The product contains walnuts and it was packaged in the wrong carton. Due to the mis-packaging the ingredient label does not have walnuts listed."
Distribution
"Distribution made to VA, KY and TN."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0942-2013 | Food Club Chocolate Chunk Brownie Mix, packaged in 21.5-oz. boxes, UPC# 36800-13486, distributed by TOPCO Associates LLC, Skokie, IL. | 25/12/21.5-oz carton cases | Class I | Terminated | 6 Feb 2013 |
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: "The product contains walnuts and it was packaged in the wrong carton. Due to the mis-packaging the ingredient label does not have walnuts listed."
What does Class I mean?
FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Where was the product distributed?
FDA's distribution pattern field reads: "Distribution made to VA, KY and TN."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 13 Feb 2014. "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.