RecallHawk
Class I Recall

Green Giant Fresh whole WHITE onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg per case) - UPC 60580600218-2.

POTANDON PRODUCE LLC

Summary

The FDA issued a Class I for Green Giant Fresh whole WHITE onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg by POTANDON PRODUCE LLC. Reason: Potential to be contaminated with Salmonella Oranienburg..

Details

Source

Food Recall

External ID

F-0115-2022

Action Date

2021-11-10

Status

Terminated

Category

food

Product Description

Green Giant Fresh whole WHITE onions in 2 lbs. flexible mesh bags, (25/2 lb. pkg per case) - UPC 60580600218-2.

Lot/Code Info: Lot number and Julian Date on 2 lb. bag tag of Whole WHITE Onions: 42562-4 RA204 42562-4 RA208 42562-4 RA209 42562-4 RA211 42562-4 RA214 42562-4 RA215 42562-4 RA217 42562-6 RA215

Quantity Affected: Total 14,050 lbs. or 281 cases (25/2 lb. pkg per case)

Reason for Recall

Potential to be contaminated with Salmonella Oranienburg.

Distribution

Distributed in ND and MN.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-22

Company

POTANDON PRODUCE LLC

Idaho Falls, ID

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

POTANDON PRODUCE LLC 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 (POTANDON PRODUCE LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does POTANDON PRODUCE LLC have FDA actions?

POTANDON PRODUCE LLC 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-0115-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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