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NATURES TOUCH FROZEN FOODS LLC Recall: Listeria monocytogenes found in a sample of this product.

United States

TerminatedClass II

Company
NATURES TOUCH FROZEN FOODS LLC
Product
Nature's Touch US frozen Organic Whole Beans, 10-oz., UPC co…
Recall date
November 1, 2017
Terminated
November 18, 2020
Source
FDA

Reason for recall

Listeria monocytogenes found in a sample of this product.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Nature's Touch US frozen Organic Whole Beans, 10-oz., UPC code 8 7366800141 Not published in this source record 13,619 Cases Best By date code range: 2017 JUN 04 - 2019 JUN 21

Distribution

  • NJ
  • NH
  • MA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0245-2018
Event ID
78472
Status
Terminated
Classification
Class II
Company
NATURES TOUCH FROZEN FOODS LLC
Product description
Nature's Touch US frozen Organic Whole Beans, 10-oz., UPC code 8 7366800141
Quantity
13,619 Cases
Reason
Listeria monocytogenes found in a sample of this product.
Recall initiation date
November 1, 2017
Report date
November 22, 2017
Classification date
Not published in this source record
Termination date
November 18, 2020
Distribution pattern
NJ, NH, MA
UPC, lot, and code information
Best By date code range: 2017 JUN 04 - 2019 JUN 21
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: NATURES TOUCH FROZEN FOODS LLC

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
New Jersey 1
New Hampshire 1
Massachusetts 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.