CRF Frozen Foods, LLC Recall: Lima Beans are recalled because they have the potential to be contaminated with Listeria monocytogenes. - F-1814-2016

🇺🇸 United States

1. May 2, 2016 - Recall initiated
2. August 3, 2016 - Reported by source
3. September 11, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1814-2016

Status

Terminated

Classification

Class I

Company

CRF Frozen Foods, LLC

Product description

Baby Lima Beans, Brand Parade, Net Wt 16 oz, UPC 5070030670 Baby Lima Beans, Safeway Kitchens, Net Wt 20 oz, UPC 2113009144 Lima Beans, Brand Signature Kitchens, Net Wt 16 oz, UPC 2113009946 Lima Beans, Brand Signature Kitchens, Net Wt 20 oz, UPC 2113009944 Baby Lima Beans, Brand VIP, Net Wt 16 oz, UPC 7007701016 Baby Lima Beans, Brand Quirch, Net Wt 14 oz, UPC 6507260150 Baby Lima Beans, Brand Quirch, Net Wt 32 oz, UPC 6507260149

Quantity

Not published in this source record

Reason

Lima Beans are recalled because they have the potential to be contaminated with Listeria monocytogenes.

Recall initiation date

May 2, 2016

Report date

August 3, 2016

Classification date

Not published in this source record

Termination date

September 11, 2017

Distribution pattern

US nationwide and in Canada & Japan.

UPC, lot, and code information

UPC 5070030670

Voluntary or mandated

Not published in this source record

Initial notification method

Not published in this source record

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: CRF Frozen Foods, LLC

Other recalls from CRF Frozen Foods, LLC

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 September 11, 2017.

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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