D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds)
Recalled by Weaver Nut Company, Inc
Food recall
Weaver Nut Company, Inc
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Weaver Nut Company, Inc has recalled D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 5, 2025 and was initiated on June 16, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), with approximately 1760 cases affected. The company behind the recall is Weaver Nut Company, Inc, based in Lebanon, PA. The FDA describes the product as: “D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.”
Why was D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds) recalled?
According to the FDA, the stated reason for the recall is: “undeclared milk allergen.” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), compare it against the product description and identifying codes (D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds) o Lot #(s) 204214-RL, 204214, 204215, 224221, 224222, 224223, 135215, 135216, 135217, 135220, 135221, 14…) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Weaver Nut Company, Inc or your local health authority.
About this recall
This recall was distributed in PA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- November 5, 2025
- Recall started
- June 16, 2025
- Distributed in
- PA
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds) recalled?+
According to the FDA: undeclared milk allergen
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds)?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0136-2026. Information last synced from the FDA on July 5, 2026.