RecallHawk
Class I Recall

Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz, 28

U.S. Tov, Inc.

Summary

The FDA issued a Class I for Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 by U.S. Tov, Inc.. Reason: Potential choking hazard; product contains konjac..

Details

Source

Food Recall

External ID

F-0865-2024

Action Date

2024-02-21

Status

Terminated

Category

food

Product Description

Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz, 28.22oz UPC Code 721557357170, 721557357187

Lot/Code Info: UPC Code 721557357156, 721557357163, 721557357170, 721557357187

Quantity Affected: 36,812 pkgs

Reason for Recall

Potential choking hazard; product contains konjac.

Distribution

U.S. distribution to the following: AK, AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, ND, NE, NH, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-04

Company

U.S. Tov, Inc.

Hayward, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (U.S. Tov, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does U.S. Tov, Inc. have FDA actions?

This is the only FDA action we have on record for U.S. Tov, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0865-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions