Grimmway Enterprises, Inc. dba Grimmway Farms Recall: Carrot products may be contaminated with Salmonella - F-0813-2021

🇺🇸 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-0813-2021

Event ID

88330

Status

Terminated

Classification

Class I

Company

Grimmway Enterprises, Inc. dba Grimmway Farms

Product description

Organic Baby Rainbow Carrots Brand name: O Organics 12 oz. (340 g) plastic bag UPC: 0 7989398162 8 12 oz. bag - Wegmans. Did not reach retail. Destroyed at DC's 12 oz. bag - GreenWise. Dis not reach retail, Destroyed at DC's

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 13 21, AUG 14 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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of February 25, 2022.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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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