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FoodRecallWatch

The Jm Smucker Company LLC Recall History

The Jm Smucker Company LLC has had 10 FDA-tracked food recalls since 2022, including 10 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
10
Years in FDA Data
Since 2022
Class I (Most Serious)
10
Most Common Reason
Salmonella contamination (10)
Latest Recall
May 20, 2022
First Recorded Recall
May 20, 2022
States Affected
49 states (nationwide)
Currently Active
0
Data Source
FDA openFDA + USDA FSIS
10
Total Recalls
10
Class I (Dangerous)
0
Class II
0
Class III

Complete Recall List (10 Records)

Every The Jm Smucker Company 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.

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, The Jm Smucker Company LLC has 10 FDA food recalls on record, including 10 Class I (dangerous) recalls. There are no active recalls at this time.

The Jm Smucker Company LLC has no active recalls at this time. However, the brand has 10 historical recalls. Always check this page for the latest recall status.

The Jm Smucker Company LLC's 10 recalls break down by severity: 10 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.

The Jm Smucker Company LLC recalls have affected 49 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).

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.