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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food
Food & Beverages/Snacks & Confections

Dragonfly Jelly Bar Handbags and Backpacks Recalled for Choking Hazard

Agency Publication Date: February 9, 2024
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Summary

U.S. Tov, Inc. is recalling approximately 36,812 packages of Dragonfly Jelly Bar Handbags and Backpacks. The recalled products include two sizes of handbag-style packaging (11.64oz and 17.63oz) and two sizes of backpack-style packaging (7.93oz and 28.22oz). These products were distributed in 38 states across the United States. The recall was initiated because the jelly bars contain konjac, which can pose a significant choking risk. No incidents or injuries have been reported to date.

Risk

The jelly bars contain konjac, a gelling agent that does not dissolve easily in the mouth. This creates a potential choking hazard because the product can become lodged in the throat and block the airway.

What You Should Do

  1. This recall affects Dragonfly Jelly Bar Handbags (11.64 oz and 17.63 oz) and Dragonfly Jelly Bar Backpacks (7.93 oz and 28.22 oz) with UPC codes 721557357156, 721557357163, 721557357170, or 721557357187.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact U.S. Tov, Inc. for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Dragonfly Jelly Bar Handbag
Variants: 11.64 oz, 17.63 oz
UPC Codes:
721557357156
721557357163
Lot Numbers:
721557357156

Recall #: F-0865-2024

Product: Dragonfly Jelly Bar Backpack
Variants: 7.93 oz, 28.22 oz
UPC Codes:
721557357170
721557357187

Recall #: F-0865-2024

Product Images

Image 1 โ€“ Product Image, Jelly Handbag, 17.63oz

Image 1 โ€“ Product Image, Jelly Handbag, 17.63oz

Image 2 โ€“ Product Image, Jelly Backpack, 7.93 oz

Image 2 โ€“ Product Image, Jelly Backpack, 7.93 oz

Image 3 โ€“ Product Image, Jelly Backpack, 28.22oz

Image 3 โ€“ Product Image, Jelly Backpack, 28.22oz

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93784
Status: Resolved
Manufacturer: U.S. Tov, Inc.
Sold By: Retailers nationwide
Manufactured In: United States
Units Affected: 36,812 pkgs
Distributed To: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Nebraska, New Hampshire, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.