Skip to main content
FoodRecallWatch

Lydia Pack 3 INC Recall History

Lydia Pack 3 INC has had 1 FDA-tracked food recall since 2024, 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
1
Years in FDA Data
Since 2024
Class I (Most Serious)
1
Most Common Reason
Mislabeling (1)
Latest Recall
Jan 19, 2024
First Recorded Recall
Jan 19, 2024
States Affected
IN, OR, WA
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
1
Total Recalls
1
Class I (Dangerous)
0
Class II
0
Class III

Complete Recall List (1 Records)

Every Lydia Pack 3 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
Jan 19, 2024Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packa...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, Lydia Pack 3 INC has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There are no active recalls at this time.

Lydia Pack 3 INC has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.

Lydia Pack 3 INC's 1 recall break down by severity: 1 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.

Lydia Pack 3 INC recalls have affected IN, OR, WA. 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).

this entity is one of the data points covered by this site’s U.S. FDA food, drug, and device recalls dataset. The detail above comes directly from the FDA openFDA enforcement-report API; the context that follows situates the headline numbers against the broader distribution across U.S. consumer-product recalls.

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.