Trader Joe's Southwestern Chopped Salad Contains: Green Cabbage, Romaine, Cotija Cheese, Roasted Pepitas, Tortilla Strip
Summary
The FDA issued a Class II for Trader Joe's Southwestern Chopped Salad Contains: Green Cabbage, Romaine, Cotija by Taylor Farms Retail Inc. Reason: Trader Joes branded Southwestern Chopped Salad Kits was found to contain the incorrect master pack. The master pack includes the allergens of soy and.
Details
Source
Food Recall
External ID
F-1258-2022
Action Date
2022-06-15
Status
Terminated
Category
food
Product Description
Trader Joe's Southwestern Chopped Salad Contains: Green Cabbage, Romaine, Cotija Cheese, Roasted Pepitas, Tortilla Strips, Green Onion, Cilantro, and a spicy Southwest Avocado Dressing Best if used by: May 26, 2022 Perishable, Keep Refrigerated Product of USA-Mexico Romaine: Salinas Contains Milk, Soy Dist. & Sold Exclusively by: Trader Joe's, Monrovia, CA 91016
Lot/Code Info: Lot code: TFGD129B18
Quantity Affected: 156 cases with 22 bags in each case
Reason for Recall
Trader Joes branded Southwestern Chopped Salad Kits was found to contain the incorrect master pack. The master pack includes the allergens of soy and pistachio. Soy was declared on the label, but pistachio was not.
Distribution
Product was shipped to two Trader Joe's DC's. Product was distributed to Fontana, CA Stockton, CA and surrounding area from these DCs.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-18
Company
Salinas, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Taylor Farms Retail Inc has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Taylor Farms Retail Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Taylor Farms Retail Inc have FDA actions?
Taylor Farms Retail Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1258-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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