Food, drugs, devices › Gilster-Mary Lee Corp.
Food recall: Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a
FDA enforcement event 70281 is a food recall by Gilster-Mary Lee Corp. of Chester, IL, initiated 13 Jan 2015 and classified Class I, with 1 product record.
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. 47% of the 607 food enforcement events initiated in 2015 carry the same class.
Status: Terminated, terminated 12 Apr 2016. 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
"Undeclared almonds"
Distribution
"US: Nationwide (AZ, CA, CT, DE, FL, GA, HI, IA, IL, IN, MA, MD, MI, MN, ND, NE, NJ, NM, NV, NY, OH, PA, SD, TX, UT, VA, WI, WV) + District of Columbia"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1806-2015 | Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a new weight of 18 oz. (1 lb. 2 oz.) 510 g. | 412 cases (4,944 cartons) | Class I | Terminated | 8 Apr 2015 |
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: "Undeclared almonds"
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: "US: Nationwide (AZ, CA, CT, DE, FL, GA, HI, IA, IL, IN, MA, MD, MI, MN, ND, NE, NJ, NM, NV, NY, OH, PA, SD, TX, UT, VA, WI, WV) + District of Columbia"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 12 Apr 2016. "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.