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Allen's Blueberry Freezer, Inc. Recall: Product tested positive for Listeria monocytogenes

United States

TerminatedClass I

Company
Allen's Blueberry Freezer, Inc.
Product
Allen's Blueberries IQF Wild Blueberries, 30 lbs. corrugated…
Recall date
October 2, 2017
Terminated
May 7, 2018
Source
FDA

Reason for recall

Product tested positive for Listeria monocytogenes

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Allen's Blueberries IQF Wild Blueberries, 30 lbs. corrugated box Not published in this source record 45330 lbs lMA - 2 thru lMA-21 and M21976

Distribution

  • New York Foreign: Canada

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0020-2018
Event ID
78210
Status
Terminated
Classification
Class I
Company
Allen's Blueberry Freezer, Inc.
Product description
Allen's Blueberries IQF Wild Blueberries, 30 lbs. corrugated box
Quantity
45330 lbs
Reason
Product tested positive for Listeria monocytogenes
Recall initiation date
October 2, 2017
Report date
October 18, 2017
Classification date
Not published in this source record
Termination date
May 7, 2018
Distribution pattern
New York Foreign: Canada
UPC, lot, and code information
lMA - 2 thru lMA-21 and M21976
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

Responsible company: Allen's Blueberry Freezer, Inc.

Other recalls from Allen's Blueberry Freezer, Inc.

FDA Recall United States TerminatedTerminated: March 4, 2021Historical recordClass I

Allen's Blueberry Freezer, Inc.

Product
Wild Sweet ALLEN'S BLUEBERRIES WILD BLUEBERRIES IQF 30 LBS.…
Published
April 10, 2019
Distribution
WA

View recall →

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.

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 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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