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CAMBRIDGE FARMS OF HANOVER LLC D Recall: Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.

United States

TerminatedClass II

Company
CAMBRIDGE FARMS OF HANOVER LLC D
Product
Giant Eagle Sweet & Savory Island Quinoa, Giant Eagle, Pitts…
Recall date
August 18, 2016
Terminated
June 30, 2017
Source
FDA

Reason for recall

Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Giant Eagle Sweet & Savory Island Quinoa, Giant Eagle, Pittsburgh, PA; 12 oz. pkgs; BB 06/10/18 Not published in this source record 450 cases, 12 units/cs. BB 06/10/2018

Distribution

  • CT
  • FL
  • MA
  • MD
  • NC
  • PA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2390-2016
Event ID
74976
Status
Terminated
Classification
Class II
Company
CAMBRIDGE FARMS OF HANOVER LLC D
Product description
Giant Eagle Sweet & Savory Island Quinoa, Giant Eagle, Pittsburgh, PA; 12 oz. pkgs; BB 06/10/18
Quantity
450 cases, 12 units/cs.
Reason
Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.
Recall initiation date
August 18, 2016
Report date
September 28, 2016
Classification date
Not published in this source record
Termination date
June 30, 2017
Distribution pattern
CT, FL, MA, MD, NC, PA
UPC, lot, and code information
BB 06/10/2018
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

Other products recalled under this same event

This recall shares FDA event ID 74976 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product
Key Foods Soup Mix Vegetables, Key Foods Stores/ Staten Isla…
Published
September 28, 2016
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product
Better Value Mix Vegetables, Federated Group, Inc./Arlington…
Published
September 28, 2016
Distribution
Multiple states

View recall →

Responsible company: CAMBRIDGE FARMS OF HANOVER LLC D

Other recalls from CAMBRIDGE FARMS OF HANOVER LLC D

FDA Recall United States Terminated Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product
Key Foods Soup Mix Vegetables, Key Foods Stores/ Staten Isla…
Published
September 28, 2016
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product
Better Value Mix Vegetables, Federated Group, Inc./Arlington…
Published
September 28, 2016
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product
The Perfect Bite Co Hawaiian Style Rice & Vegetable Blend, 4…
Published
September 28, 2016
Distribution
Multiple states

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Connecticut 1
Florida 1
Massachusetts 1
Maryland 1
North Carolina 1
Pennsylvania 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.