CLASS I Food recall · Reported 2 Jan 2019 · FDA Enforcement Report

Tamy Pop recalled by Procesadora de Dulces

Procesadora de Dulces Tipicos is recalling Tamy Pop. The recall was initiated on 7 Dec 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC Code: 878631001358; Lot numbers 18244, 18258, 18274, 18288, 1847
Quantity recalled417 cases

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-0760-2019
FDA event ID
81724
Recalling firm
Procesadora de Dulces Tipicos, Guadalajara
Classification
Class I
Status
Terminated
Recall initiated
7 Dec 2018
FDA classified
28 Jan 2019
Reported
2 Jan 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Soy
Product category
Other

Timeline

7 Dec 2018Recall initiated by company
2 Jan 2019Published in enforcement report+26 days
28 Jan 2019Classified by FDA+26 days

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

Reason for recall

Undeclared soy in candy

Product as listed by the FDA

Tamy Pop 18 pieces Net Wt. 1 lb. 15.7 oz. packaged in a clear plastic jar, 6 jars per case

Where it was distributed

United States

Questions about this recall

Why was it recalled?

Undeclared soy in candy

Which lots are affected?

UPC Code: 878631001358; Lot numbers 18244, 18258, 18274, 18288, 1847

Where was it sold?

United States

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

Other products in this recall event

3 other products · FDA event 81724

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