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FoodRecallWatch

Eillien's Candies, INC. Recall History

Eillien's Candies, INC. has had 2 FDA-tracked food recalls since 2016, including 2 Class I recalls (most serious). The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.

Key Facts

Total Recalls
2
Years in FDA Data
2016–2021
Class I (Most Serious)
2
Most Common Reason
Undeclared allergens (1)
Latest Recall
Jul 2, 2021
First Recorded Recall
May 23, 2016
States Affected
11 states (nationwide)
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
2
Total Recalls
2
Class I (Dangerous)
0
Class II
0
Class III

Complete Recall List (2 Records)

Every Eillien's Candies, INC. recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.

DateProductClassStatus
Jul 2, 2021Blain's Farm & Fleet Select Dark Chocolate Amaretto Pecan...Class ITerminated
May 23, 2016HOLIDAY PANTRY, RAISIN & NUT , NET WT. 9 OZ(255 G), UPC...Class ITerminated

Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.

Frequently Asked Questions

Yes, Eillien's Candies, INC. has 2 FDA food recalls on record, including 2 Class I (dangerous) recalls. There are no active recalls at this time.

Eillien's Candies, INC. has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.

Eillien's Candies, INC.'s 2 recalls break down by severity: 2 Class I (may cause serious health issues), 0 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.

Eillien's Candies, INC. recalls have affected 11 states (nationwide distribution). Check individual recall entries for specific distribution details.

Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).

The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.

Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.

Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.