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FoodRecallWatch

Diamond Crystal Brands INC Recall History

1 Active Recall

Diamond Crystal Brands INC has had 5 FDA-tracked food recalls since 2017, including 1 Class I recall (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
2017–2019
Class I (Most Serious)
1
Most Common Reason
Foreign material (2)
Latest Recall
Aug 30, 2019
First Recorded Recall
Feb 17, 2017
States Affected
54 states (nationwide)
Currently Active
1
Data Source
FDA openFDA + USDA FSIS
5
Total Recalls
1
Class I (Dangerous)
4
Class II
0
Class III

Complete Recall List (5 Records)

Every Diamond Crystal Brands 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.

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, Diamond Crystal Brands INC has 5 FDA food recalls on record, including 1 Class I (dangerous) recall. There is currently 1 active recall.

Diamond Crystal Brands INC currently has 1 active recall. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.

Diamond Crystal Brands INC's 5 recalls break down by severity: 1 Class I (may cause serious health issues), 4 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.

Diamond Crystal Brands INC recalls have affected 54 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.

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.