Tyson Foods Discovery Center FDA recall records

The FDA has published 5 food recall enforcement records naming Tyson Foods Discovery Center between 2018 and 2018, covering 2 separate recall events. The firm is recorded in Arkansas. Data last updated 2 September 2026.

Records of 29,386
5
Share of all recalls
0%
Class I of 5
1
Reported between
2018 to 2018

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 5 records cover 2 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

1 of these records are Class I, 4 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

What was recalled for

A single record can name more than one hazard, so these counts overlap.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 5 records.
ReportedProductFirmReasonClass
2018-11-14Pierre Philly Style Chicken Sandwich, item 1238, 12 units packaged per case Net Wt. 4.99 LBS (2.27 kg) KEEP FROZENTyson Foods Discovery CenterThe ingredient supplier initiated a recall due to the potential contamination of Listeria monocytogenes and Salmonella.Class II
2018-11-14Steak-EZE Philly Cheesesteak Sandwich, item 06433, Net Wt 5.15 OZ., 4 sandwiches per case KEEP FROZENTyson Foods Discovery CenterThe ingredient supplier initiated a recall due to the potential contamination of Listeria monocytogenes and Salmonella.Class II
2018-11-14TGIF All American Slider, item 5461, 4 cartons of 4 sandwiches per case NET WT 10 OZ KEEP FROZENTyson Foods Discovery CenterThe ingredient supplier initiated a recall due to the potential contamination of Listeria monocytogenes and Salmonella.Class II
2018-11-14Pierre Philly Style Cheesesteak Sandwich, item 1125, 12 units packaged per case Net Wt. 4.65 LBS (2.11 kg) KEEP FROZENTyson Foods Discovery CenterThe ingredient supplier initiated a recall due to the potential contamination of Listeria monocytogenes and Salmonella.Class II
2018-05-23Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOY FLOUR),***RICE FLOUR,***SUNFLOWER AND/OR SOY LECITHIN***CONTAINS: SOY DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS SAN DIEGO, CA 92154 UPC 0 89947 30206 4Tyson Foods Discovery CenterThe firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.Class I

Questions

How many FDA recalls has Tyson Foods Discovery Center had?
The FDA has published 5 food recall enforcement records naming Tyson Foods Discovery Center between 2018 and 2018. Those records cover 2 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.