CLASS I Food recall · Reported 21 Feb 2024 · FDA Enforcement Report

Dragonfly Jelly Bar Handbag recalled by U.S. Tov

U.S. Tov is recalling Dragonfly Jelly Bar Handbag, distributed in 38 states. The recall was initiated on 4 Jan 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC Code 721557357156, 721557357163, 721557357170, 721557357187
Quantity recalled36,812 pkgs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0865-2024
FDA event ID
93784
Recalling firm
U.S. Tov, Hayward, CA
Classification
Class I
Status
Terminated
Recall initiated
4 Jan 2024
FDA classified
9 Feb 2024
Reported
21 Feb 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Choking Hazard
Product category
Fish

Timeline

4 Jan 2024Recall initiated by company
9 Feb 2024Classified by FDA+36 days
21 Feb 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential choking hazard; product contains konjac.

Product as listed by the FDA

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

Where it was distributed

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.

AlaskaAlabamaArkansasArizonaCaliforniaColoradoFloridaGeorgiaIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouri

Questions about this recall

Is Dragonfly Jelly Bar Handbag recalled?

Yes. U.S. Tov recalled Dragonfly Jelly Bar Handbag on 4 Jan 2024. The recall is Class I and its status is Terminated. Recall number F-0865-2024.

Why was it recalled?

Potential choking hazard; product contains konjac.

Which lots are affected?

UPC Code 721557357156, 721557357163, 721557357170, 721557357187

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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