Marketside Tomato Bisque Soup Kit Recall
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Cuisine Kettle is recalling Marketside Tomato Bisque Soup Kit due to a presumptive positive test result for Listeria monocytogenes.
Reading this FDA recall beyond the headline
This notice was issued by FDA on September 8, 2026 and geographically references IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, AR. The FDA classifies this as a Class II recall, with the stated reason "Product had a presumptive positive test result for Listeria monocytogenes", distributed the recalled product was distributed to the following states: il, nv, nm, ca, ok, tx, pa, oh, nc, ny, ga, and ar.. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
A quick skim tells you whether this affects you directly; a closer read tells you more. Check the scope, the source, and how recent the record is, then weigh it against related notices rather than treating any single one as a trend.
The original agency source is linked below so you can verify this record directly before acting on it. Its related labels are recall, product-safety, fda, Food.
What Happened
Cuisine Kettle is voluntarily recalling Marketside Tomato Bisque Soup Kit after a presumptive positive test result for Listeria monocytogenes.
Which Products Are Affected
The recall involves Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), UPC 1 94346474004. Must Keep Refrigerated. Best By/Use By: 8/22/2026. A total of 540 cases were distributed to IL, NV, NM, CA, OK, TX, PA, OH, NC, NY, GA, and AR. The recall number is H-1271-2026.
What You Should Do
Consumers should not consume the product and should return it to the place of purchase or contact the recalling firm for further instructions.
Why This Matters
Listeria monocytogenes can cause serious illness, particularly in vulnerable populations.
Source
FDA recall H-1271-2026, report date 20260902.
Original source: FDA Official Notice ↗
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