All American Slider (TGIF) – potential contamination (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
TGIF All American Slider, item 5461, 4 cartons of 4 sandwiches per case NET WT 10 OZ KEEP FROZEN
Brand
Tyson Foods Discovery Center
Lot Codes / Batch Numbers
Lots : 1482755901, 1482705901, 1482685901, 1482675901, 1482645901, 1482635901, 1482295901, 1482285901, 1482215901, 1482065901, 1482055901, 1481835901, 1481695901, 1481665901, 1481655901, 1481415901, 1481305901, 1481275901, 1481235901, 1481005901, 1480815901, 1480795901, 1480665901, 1480655901, 1480535901, 1480525901, 1480395901, 1480385901, 1480235901
Products Sold
Lots : 1482755901, 1482705901, 1482685901, 1482675901, 1482645901, 1482635901, 1482295901, 1482285901, 1482215901, 1482065901, 1482055901, 1481835901, 1481695901, 1481665901, 1481655901, 1481415901, 1481305901, 1481275901, 1481235901, 1481005901, 1480815901, 1480795901, 1480665901, 1480655901, 1480535901, 1480525901, 1480395901, 1480385901, 1480235901
Tyson Foods Discovery Center is recalling TGIF All American Slider, item 5461, 4 cartons of 4 sandwiches per case NET WT 10 OZ KEEP FROZEN due to The ingredient supplier initiated a recall due to the potential contamination of Listeria monocytogenes and Salmonella.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The ingredient supplier initiated a recall due to the potential contamination of Listeria monocytogenes and Salmonella.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026