Food recall: King of Pops Key Lime Pie, frozen flavored pop cycle, Net Wt. 3.2oz., Hand Made by King of Pops, 4845 Chateau Ave., Unit
FDA enforcement event 68804 is a food recall by Coastal KOP LLC dba King of Pops of Charleston, SC, initiated 14 Jul 2014 and classified Class II, with 2 product records.
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. 41% of the 573 food enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 13 Jun 2017. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Coastal KOP LLC dba King of Pops.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Coastal KOP LLC dba King of Pops, Charleston, SC.
Reason for recall
"Undeclared Allergens: Soy, Wheat"
Distribution
"SC"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-2240-2014 | King of Pops Key Lime Pie, frozen flavored pop cycle, Net Wt. 3.2oz., Hand Made by King of Pops, 4845 Chateau Ave., Unit D, Charleston, SC 29405 | 100 3.2-oz units total for both flavors | Class II | Terminated | 6 Aug 2014 |
| F-2241-2014 | King of Pops Banana Puddin', frozen flavored pop cycle, Net Wt. 3.2oz., Hand Made by King of Pops, 4845 Chateau Ave., Unit D, Charleston, SC 29405 | 100 3.2-oz units total for both flavors | Class II | Terminated | 6 Aug 2014 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Undeclared Allergens: Soy, Wheat"
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: "SC"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 13 Jun 2017. "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.