1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit

Bendon Publishing has recalled 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 7, 2026 and was initiated on December 3, 2025. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).

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 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, with approximately 39,171 individual units (TOTAL) affected. The company behind the recall is Bendon Publishing, based in Ashland, OH. The FDA describes the product as: “1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219643846, Distributed by Bendon, Inc. 2) Mickey Mouse Heart-Shaped Gummies, Mixed Fruit, Net Wt. 7 oz (200g), packaged in a…”

Why was 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit recalled?

According to the FDA, the stated reason for the recall is: “Unapproved color additive - chlorophyllin copper complex.” In plain terms, this recall relates to an unapproved substance or additive.

This type of recall involves an ingredient or additive — such as a color, preservative, or other substance — that is not approved for use in the food as sold under U.S. rules. It does not automatically mean the product is harmful, but it does mean it does not meet current food regulations.

What should you do?

If you think you may have bought 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, compare it against the product description and identifying codes (1) Lot# 3514-8A; Best Before 08/19/2027; Internal Item#: PC64384-WMPDQ 2) Lot# 3514-8B; Best Before 08/19/2027; Internal Item#: PC64385-WMPDQ 3) Lot# 3514-8C;…) before using it.

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 Bendon Publishing or your local health authority.

About this recall

This recall was distributed in OH. 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.