FDA recall record

Bendon Publishing 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net Wt recall — FDA H-0350-2026

Unapproved color additive - chlorophyllin copper complex

Class IIIclassification
H-0350-2026official record ID
Jan 7, 2026report date

Recall record at a glance

Official recordH-0350-2026
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBendon Publishing
Report dateJan 7, 2026
Recall initiation dateDec 3, 2025
Quantity39,171 individual units (TOTAL)
LocationAshland, OH, United States

Official product description

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 cardboard box with heart-shaped top, UPC 805219643853, Distributed by Bendon, Inc. 3) Stitch Heart-Shaped Gummies, Tropical, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219643860, Distributed by Bendon, Inc. 4) SpongeBob Squarepants Heart-Shaped Gummy Candy, Tropical, Net Wt. 7 oz (200g), packaged in a cardboard box with heart-shaped top, UPC 805219644225, Distributed by Bendon, Inc. 5) Toy Story Multipack Size Gummies, Mixed Fruit, Net Wt. 6.35 oz (180g), packaged in a plastic bag containing 20 mini size packs (0.4 oz each), UPC 805219643914, Distributed by Bendon, Inc.

Why the product was recalled

Unapproved color additive - chlorophyllin copper complex

Distribution information

Distributors in FL, MN, TX, WA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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