RecallHawk
Class II Recall

Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: 1. Produce Code 448007, 2-5 lb. bags pe

G.O. Corporation

Summary

The FDA issued a Class II for Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: by G.O. Corporation. Reason: Romaine lettuce may be contaminated with deer feces..

Details

Source

Food Recall

External ID

F-1427-2023

Action Date

2023-08-23

Status

Ongoing

Category

food

Product Description

Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: 1. Produce Code 448007, 2-5 lb. bags per shipping case, 2. Produce Code 448007, 4-5 lb. bags per shipping case, 3. Produce Code 448110, 4-5 lb. bags per shipping case.

Lot/Code Info: Lot Codes: 1. 130209, 130212; 2. 130209; 3. 130212.

Quantity Affected: 23,186 lbs. total

Reason for Recall

Romaine lettuce may be contaminated with deer feces.

Distribution

IA, MN, ND, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-01

Company

G.O. Corporation

Minneapolis, MN

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

G.O. Corporation has 11 FDA actions in our database, including 11 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 (G.O. Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does G.O. Corporation have FDA actions?

G.O. Corporation has 11 FDA actions in our database, including 11 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1427-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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