Doehler North America, INC. Recall History
Doehler North America, INC. has had 1 FDA-tracked food recall since 2025, 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 2025
- Class I (Most Serious)
- 1
- Most Common Reason
- Listeria contamination (1)
- Latest Recall
- Jul 25, 2025
- First Recorded Recall
- Jul 25, 2025
- States Affected
- 44 states (nationwide)
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Doehler North America, 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.
| Date | Product | Class | Status |
|---|---|---|---|
| Jul 25, 2025 | Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-... | Class I | Active |
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, Doehler North America, INC. has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There is currently 1 active recall.
Doehler North America, 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.
Doehler North America, 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.
Doehler North America, INC. recalls have affected 44 states (nationwide distribution). Check individual recall entries for specific distribution details.
Related
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.