RecallHawk
Class I Recall

Bacon Avocado Wrap, Net Wt 9.9oz. Keep Refrigerated. UPC 7 95631-81038 7. Containing Flour Tortilla,Carrots, Lettu

RUSS DAVIS WHOLESALE

Summary

The FDA issued a Class I for Bacon Avocado Wrap, Net Wt 9.9oz. Keep Refrigerated. UPC 7 95631-81038 7. by RUSS DAVIS WHOLESALE. Reason: Cucumbers have potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-0369-2025

Action Date

2025-01-08

Status

Terminated

Category

food

Product Description

Bacon Avocado Wrap, Net Wt 9.9oz. Keep Refrigerated. UPC 7 95631-81038 7. Containing Flour Tortilla,Carrots, Lettuce, Cheddar Cheese, Cucumber, Guacamole, Bacon Bits, Ranch Dressing, Spinach, Cream Cheese. Sold under the following brands: 1. Crazy Fresh 2. quick & easy, Meals

Lot/Code Info: Lot Codes: X7547814, X7550037, X7554119, X7554784, X7556770, X7558868. Sell By Dates: November 5 - November 15, 2024

Quantity Affected: 491 units

Reason for Recall

Cucumbers have potential to be contaminated with Salmonella.

Distribution

IA, IL, KS, MI, MN, MT, ND, NE, SD, WI, WY

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-01

Company

RUSS DAVIS WHOLESALE

Saint Paul, MN

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 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.

RUSS DAVIS WHOLESALE has 5 FDA actions in our database, including 5 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 (RUSS DAVIS WHOLESALE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does RUSS DAVIS WHOLESALE have FDA actions?

RUSS DAVIS WHOLESALE has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0369-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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