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FoodRecallWatch

Craftmark Bakery, LLC Recall History

Craftmark Bakery, LLC has had 2 FDA-tracked food recalls since 2025. 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
Since 2025
Class I (Most Serious)
0
Most Common Reason
Foreign material (2)
Latest Recall
Mar 27, 2025
First Recorded Recall
Mar 27, 2025
States Affected
CA, IL, MD
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
2
Total Recalls
0
Class I (Dangerous)
2
Class II
0
Class III

Complete Recall List (2 Records)

Every Craftmark Bakery, LLC 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
Mar 27, 20255000108 OATMEAL RAISIN COOKIE DOUGH, 6 poly bags of 30 fr...Class IITerminated
Mar 27, 20255000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough, ...Class IITerminated

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, Craftmark Bakery, LLC has 2 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.

Craftmark Bakery, LLC has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.

Craftmark Bakery, LLC's 2 recalls break down by severity: 0 Class I (may cause serious health issues), 2 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.

Craftmark Bakery, LLC recalls have affected CA, IL, MD. 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.

The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.

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.