RecallHawk
Class I Recall

Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shelf life, packaged into plastic containers

Sprouts Farmers Market

Summary

The FDA issued a Class I for Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shel by Sprouts Farmers Market. Reason: Product may contain Listeria monocytogenes..

Details

Source

Food Recall

External ID

H-0088-2026

Action Date

2025-10-29

Status

Terminated

Category

food

Product Description

Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shelf life, packaged into plastic containers at Deli counter and into 16oz plastic grab & go containers, weight dependent on customer request, UPC 2-15587-00000 (from service case) and 2-15786-00000 (from Grab & Go), Sprouts Farmers Market 5455 E High St., Suite 111 Phoenix, AZ 85054.

Lot/Code Info: Use by Date range is 10/10/25 - 10/29/25.

Quantity Affected: 4896 pasta kits

Reason for Recall

Product may contain Listeria monocytogenes.

Distribution

Distributed in AL, AZ, CA, CO, DE, FL, GA, KS, LA, MD, MO, NC, NJ, NM, NV, OK, PA, SC, TN, TX, UT, VA, WA, and WY.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-08

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Sprouts Farmers Market has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Sprouts Farmers Market) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sprouts Farmers Market have FDA actions?

Sprouts Farmers Market has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0088-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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