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Hart Freeze pack, LLC Recall: potential contamination with Listeria Monocytogenes

United States

TerminatedClass II

Company
Hart Freeze pack, LLC
Product
3/8" diced IQF zucchini in 45 pound poly lined carton
Recall date
November 5, 2019
Terminated
April 2, 2020
Source
FDA

Reason for recall

potential contamination with Listeria Monocytogenes

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
3/8" diced IQF zucchini in 45 pound poly lined carton Not published in this source record 114,480 pounds E1565 0816191; E1566 0816191; E1572 0816192

Distribution

  • CA
  • OH

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0710-2020
Event ID
84449
Status
Terminated
Classification
Class II
Company
Hart Freeze pack, LLC
Product description
3/8" diced IQF zucchini in 45 pound poly lined carton
Quantity
114,480 pounds
Reason
potential contamination with Listeria Monocytogenes
Recall initiation date
November 5, 2019
Report date
February 26, 2020
Classification date
Not published in this source record
Termination date
April 2, 2020
Distribution pattern
CA, OH
UPC, lot, and code information
E1565 0816191; E1566 0816191; E1572 0816192
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Hart Freeze pack, LLC

Other recalls from Hart Freeze pack, LLC

FDA Recall United States Terminated Historical recordClass II

Hart Freeze pack, LLC

Product
Pictsweet Farms Steam'ables Asparagus Spears 8oz. pouch, 10…
Published
December 5, 2018
Distribution
MI

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
California 1
Ohio 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.