CLASS I Food recall · Reported 22 Jan 2014 · FDA Enforcement Report

Candy Sweet Spots (3 display packages/case recalled by Bee International

Bee International is recalling Candy Sweet Spots (3 display packages/case, distributed nationwide in the US. The recall was initiated on 12 Dec 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesMfg code: 2158613 (Date of manufacture: 158 day of 2012) Mfg code: 2335613 (Date of manufacture: 335 day of 2012)

Quantity recalled4481 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-1403-2014
FDA event ID: 67077
Recalling firm: Bee International, Chula Vista, CA
Classification: Class I
Status: Terminated
Recall initiated: 12 Dec 2013
FDA classified: 10 Jan 2014
Reported: 22 Jan 2014
Type: Voluntary: Firm initiated
Customers notified by: Press Release
Reason category: Undeclared Egg
Product category: Candy

Timeline

12 Dec 2013	Recall initiated by company
10 Jan 2014	Classified by FDA	+29 days
22 Jan 2014	Published 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

Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen.

Product as listed by the FDA

Candy Sweet Spots, 2oz. (3 display packages/case; 12-2oz packages/display case). UPC 0-73563-00471-6

Where it was distributed

Nationwide in US and Canada.

Nationwide

Questions about this recall

Is Candy Sweet Spots (3 display packages/case recalled?

Yes. Bee International recalled Candy Sweet Spots (3 display packages/case on 12 Dec 2013. The recall is Class I and its status is Terminated. Recall number F-1403-2014.

Why was it recalled?

Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen.

Which lots are affected?

Mfg code: 2158613 (Date of manufacture: 158 day of 2012) Mfg code: 2335613 (Date of manufacture: 335 day of 2012)

Where was it sold?

Nationwide in US and Canada.

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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