Class I Recall

Egg &Cheese Curd Snack/Power Box. Cheese Curds, Hard-Cooked Egg, Apple Wedges, Peanut Butter & Lettuce. Keep Refrigera

Summary

The FDA issued a Class I for Egg &Cheese Curd Snack/Power Box. Cheese Curds, Hard-Cooked Egg, Apple Wedges, by Bix Produce Company LLC. Reason: Potential Salmonella contamination..

Details

Source

Food Recall

External ID

F-1285-2022

Action Date

2022-06-22

Status

Terminated

Product Description

Egg &Cheese Curd Snack/Power Box. Cheese Curds, Hard-Cooked Egg, Apple Wedges, Peanut Butter & Lettuce. Keep Refrigerated. Net Weight (142g/5.0 oz). UPC 46709-00570. Manufactured by: BIX Produce Company, 3600 Centerville Rd, Little Canada, MN 55117

Lot/Code Info: Use by Date Range: 4/18/2022 - 05/31/2022 Lot Numbers: P2370420-00, P2370448-00, P2371263-00, P2371953-00, P2372708-00, P2372737-00, P2373486-00, P2374677-00, P2374708-00, P2375483-00, P2375515-00, P2376274-00, P2376996-00, P2377028-00, P2377855-00, P2379202-00, P2379234-00, P2380037-00, P2380882-00, P2380912-00, P2381701-00, P2381733-00, P2382581-00, P2382614-00, P2383921-00, P2383953-00, P2384830-00, P2385676-00, P2385709-00, P2386519-00, P2386551-00, P2387386-00, P2387419-00, P2388742-00, P2388774-00, P2389607-00, P2389640-00, P2390429-00, P2390460-00, P2391243-00, P2391274-00, P2392109-00, P2393405-00, P2393438-00, P2394288-00, P2395102-00, P2395132-00, P2395919-00, P2395948-00, P2396743-00, P2398020-00, P2398051-00.

Quantity Affected: 666 units

Reason for Recall

Potential Salmonella contamination.

Distribution

IA, MN, ND, SD, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-24

Company

Bix Produce Company LLC

Little Canada, 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 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Bix Produce Company LLC has 4 FDA actions in our database, including 4 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 (Bix Produce Company LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bix Produce Company LLC have FDA actions?

Bix Produce Company LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1285-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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