RecallHawk
Class II Recall

Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386) packed in corrugated boxes with an inner plastic bag (6, 2lb

Get Fresh Produce, Inc.

Summary

The FDA issued a Class II for Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386) packed in corrugated by Get Fresh Produce, Inc.. Reason: Product may be contaminated with deer feces..

Details

Source

Food Recall

External ID

F-1432-2023

Action Date

2023-08-23

Status

Terminated

Category

food

Product Description

Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386) packed in corrugated boxes with an inner plastic bag (6, 2lb bags per case)

Lot/Code Info: Lots: X0194838 X0194927

Quantity Affected: 1,404 pounds or 117 finished cases

Reason for Recall

Product may be contaminated with deer feces.

Distribution

Illinois and Florida

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-02

Company

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.

Get Fresh Produce, Inc. has 2 FDA actions in our database, including 2 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 (Get Fresh Produce, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Get Fresh Produce, Inc. have FDA actions?

Get Fresh Produce, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1432-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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