Severity
Critical
FDA Food recall · Reported January 22, 2014
Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen.
The recall
Bee International, Inc. issued this critical-severity FDA Food recall — Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen..
Sourced from official FDA Food enforcement records. Verify recall #F-1403-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1403-2014) was formally reported on January 22, 2014, with the manufacturer initiating the action on December 12, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Bee International, Inc. is listed as the recalling firm, operating out of Chula Vista, CA. Federal records list the affected scope as 4481 cases.
The documented reason for this recall is: Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen. Distribution data in the federal record shows the product reached: Nationwide in US and Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category — 25,414 food recalls on record
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified high severity.
Severity
Critical
Affected scope
4481 cases
Related Recalls
6
6 from same agency
Candy Sweet Spots, 2oz. (3 display packages/case; 12-2oz packages/display case). UPC 0-73563-00471-6
Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1403-2014 |
| Date reported | January 22, 2014 |
| Date initiated | December 12, 2013 |
| Recalling firm | Bee International, Inc. |
| Firm location | Chula Vista, CA |
| Affected scope | 4481 cases |
| Distribution | Nationwide in US and Canada. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
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This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported January 22, 2014.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.