CLASS II Food recall · Reported 26 Feb 2020 · FDA Enforcement Report

3/8" diced IQF zucchini recalled by Hart Freeze Pack

Hart Freeze Pack is recalling 3/8" diced IQF zucchini, distributed in California, Ohio. The recall was initiated on 5 Nov 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesE1565 0816191; E1566 0816191; E1572 0816192
Quantity recalled114,480 pounds

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0710-2020
FDA event ID
84449
Recalling firm
Hart Freeze Pack, Hart, MI
Classification
Class II
Status
Terminated
Recall initiated
5 Nov 2019
FDA classified
14 Feb 2020
Reported
26 Feb 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Other

Timeline

5 Nov 2019Recall initiated by company
14 Feb 2020Classified by FDA+101 days
26 Feb 2020Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

potential contamination with Listeria Monocytogenes

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

3/8" diced IQF zucchini in 45 pound poly lined carton

Where it was distributed

CA, OH

CaliforniaOhio

Questions about this recall

Why was it recalled?

potential contamination with Listeria Monocytogenes

Which lots are affected?

E1565 0816191; E1566 0816191; E1572 0816192

Where was it sold?

CA, OH

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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