Grimmway Enterprises, Inc. dba Grimmway Farms Recall: Carrot products may be contaminated with Salmonella

🇺🇸 United States

1. July 19, 2021 - Recall initiated
2. August 11, 2021 - Reported by source
3. February 25, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0811-2021

Event ID

88330

Status

Terminated

Classification

Class I

Company

Grimmway Enterprises, Inc. dba Grimmway Farms

Product description

Shredded Carrots Brand name: Grimmway Farms 10 oz. (284g) plastic bag UPC: 0 7878350610 1 10 oz. plastic bags - Kroger - did not reach retail. Destroyed at DC's 10 oz. plastic bags - LIDL - Did not reach retail. Destroyed at DC's 5 lb. bags - Food Service - Brand Names - Grimmway Farms, Markon, Cross Valley Also sold to bulk customers: 500 lb. bags

Quantity

62.582 cases, 1,709,767 lbs (total)

Reason

Carrot products may be contaminated with Salmonella

Recall initiation date

July 19, 2021

Report date

August 11, 2021

Classification date

Not published in this source record

Termination date

February 25, 2022

Distribution pattern

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

UPC, lot, and code information

Best if Used by: AUG 09 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.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 88330 with 7 other product entries in Public Health Trace.

Responsible company: Grimmway Enterprises, Inc. dba Grimmway Farms

Other recalls from Grimmway Enterprises, Inc. dba Grimmway Farms

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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