RecallHawk
Class I Recall

Organic Cut and Peeled Baby Carrots Brand name: Bunny Luv 1 lb.(454 g) plastic bag UPC: 0 3338390205 0;

Grimmway Enterprises, Inc. dba Grimmway Farms

Summary

The FDA issued a Class I for Organic Cut and Peeled Baby Carrots Brand name: Bunny Luv 1 lb.(454 g) pl by Grimmway Enterprises, Inc. dba Grimmway Farms. Reason: Carrot products may be contaminated with Salmonella.

Details

Source

Food Recall

External ID

F-0810-2021

Action Date

2021-08-11

Status

Terminated

Category

food

Product Description

Organic Cut and Peeled Baby Carrots Brand name: Bunny Luv 1 lb.(454 g) plastic bag UPC: 0 3338390205 0;

Lot/Code Info: Bunny Luv: 1 lb. bag - Best if Used by: AUG 17 21, AUG 20 21: All of the products in this table have a 9-character lot code beginning with 195, 196 or 197 and ending in BF or SP printed on the bag. For example, 1952023BF.

Quantity Affected: 62.582 cases, 1,709,767 lbs (total)

Reason for Recall

Carrot products may be contaminated with Salmonella

Distribution

Nationwide. Product also shipped to Canada but destroyed before it entered retail stores.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-07-19

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

Grimmway Enterprises, Inc. dba Grimmway Farms has 13 FDA actions in our database, including 13 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 (Grimmway Enterprises, Inc. dba Grimmway Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Grimmway Enterprises, Inc. dba Grimmway Farms have FDA actions?

Grimmway Enterprises, Inc. dba Grimmway Farms has 13 FDA actions in our database, including 13 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0810-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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