Food recall: 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds), 25lb Bulk Cases Packaged into Various Size Units After distri
FDA enforcement event 97105 is a food recall by Weaver Nut Company, Inc of Lebanon, PA, initiated 16 Jun 2025 and classified Class I, with 2 product records.
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 569 food enforcement events initiated in 2025 carry the same class.
Status: Terminated, terminated 1 Sep 2026. Initiation: voluntary: firm initiated. Weaver Nut Company, Inc has 2 enforcement events on this register, with a median of 2 product records 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
Weaver Nut Company, Inc, Lebanon, PA.
Reason for recall
"undeclared milk allergen"
Distribution
"The aduterated product was distributed to the following states: NY, PA, GA, OH, NJ, NH, VA, MD, LA, MI, NC, WV, MN, AZ"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-0135-2026 | 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution. | 849 cases | Class I | Terminated | 5 Nov 2025 |
| H-0136-2026 | D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution. | 1760 cases | Class I | Terminated | 5 Nov 2025 |
Context
Other enforcement events for Weaver Nut Company, Inc
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 16 Jun 2025 | Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases | Food | Class I | 2 |
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "undeclared milk allergen"
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: "The aduterated product was distributed to the following states: NY, PA, GA, OH, NJ, NH, VA, MD, LA, MI, NC, WV, MN, AZ"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 1 Sep 2026. "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.