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FoodRecallWatch

Pacific Coast Fruit Company Recall History

Pacific Coast Fruit Company has had 5 FDA-tracked food recalls since 2012, including 5 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
5
Years in FDA Data
2012–2017
Class I (Most Serious)
5
Most Common Reason
Listeria contamination (3)
Latest Recall
Oct 20, 2017
First Recorded Recall
Aug 31, 2012
States Affected
IN, OR, WA, AK, ID
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
5
Total Recalls
5
Class I (Dangerous)
0
Class II
0
Class III

Complete Recall List (5 Records)

Every Pacific Coast Fruit Company recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.

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, Pacific Coast Fruit Company has 5 FDA food recalls on record, including 5 Class I (dangerous) recalls. There are no active recalls at this time.

Pacific Coast Fruit Company has no active recalls at this time. However, the brand has 5 historical recalls. Always check this page for the latest recall status.

Pacific Coast Fruit Company's 5 recalls break down by severity: 5 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.

Pacific Coast Fruit Company recalls have affected IN, OR, WA, AK, ID. 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.

For readers using this page as a decision input, the related-entity pages elsewhere on the site provide the comparison set. The most useful comparison for this entity is typically a peer within U.S. consumer-product recalls with similar size, similar exposure, or similar geography — not the national-level summary alone.