RecallHawk
Class I Recall

Green Giant Fresh brand, Whole WHITE Onions packaged in 2 lb. flexible mesh bags, UPC 60580600218-2.

POTANDON PRODUCE LLC

Summary

The FDA issued a Class I for Green Giant Fresh brand, Whole WHITE Onions packaged in 2 lb. flexible mesh bags by POTANDON PRODUCE LLC. Reason: Salmonella Oranienburg. Products are supplied by Keeler Family Farm..

Details

Source

Food Recall

External ID

F-0184-2022

Action Date

2021-11-24

Status

Terminated

Category

food

Product Description

Green Giant Fresh brand, Whole WHITE Onions packaged in 2 lb. flexible mesh bags, UPC 60580600218-2.

Lot/Code Info: Lot # and Julian Date on bag tag of whole WHITE onions in 2 lbs. bag: 42542-3 RA197 42542-3 RA196 42542-3 RA200 42542-3 RA201 42542-3 RA202 ADDITIONAL LOT #: 139008.

Quantity Affected: Total 10,860 lbs. or 198 cases (25/2 lb. pkg. per case) and 40 cases (12/2 lb. pkg per case).

Reason for Recall

Salmonella Oranienburg. Products are supplied by Keeler Family Farm.

Distribution

distributed in MN and ND.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-25

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 88 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-0184-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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