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FoodRecallWatch

Canteen INC. DBA Mg Foods, INC. Recall History

6 Active Recalls

Canteen INC. DBA Mg Foods, INC. has had 6 FDA-tracked food recalls since 2021, including 6 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
6
Years in FDA Data
Since 2021
Class I (Most Serious)
6
Most Common Reason
Listeria contamination (6)
Latest Recall
Mar 2, 2021
First Recorded Recall
Mar 2, 2021
States Affected
GA, NC, SC, WV
Currently Active
6
Data Source
FDA openFDA + USDA FSIS
6
Total Recalls
6
Class I (Dangerous)
0
Class II
0
Class III

Complete Recall List (6 Records)

Every Canteen INC. DBA Mg Foods, 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, Canteen INC. DBA Mg Foods, INC. has 6 FDA food recalls on record, including 6 Class I (dangerous) recalls. There are currently 6 active recalls.

Canteen INC. DBA Mg Foods, INC. currently has 6 active recalls. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.

Canteen INC. DBA Mg Foods, INC.'s 6 recalls break down by severity: 6 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.

Canteen INC. DBA Mg Foods, INC. recalls have affected GA, NC, SC, WV. 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.

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.