CLASS I Food recall · Reported 8 Mar 2017 · FDA Enforcement Report

Organic IQF Dark Sweet Cherries, 900 cartons per lot recalled

Sunrise Growers is recalling Organic IQF Dark Sweet Cherries, 900 cartons per lot, distributed in California. The recall was initiated on 17 Feb 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSWCB62071 PTR160495-28 SWCB62072 PTR160495-28
Quantity recalled1800 cases

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-1562-2017
FDA event ID
76520
Recalling firm
Sunrise Growers, Placentia, CA
Classification
Class I
Status
Terminated
Recall initiated
17 Feb 2017
FDA classified
2 Mar 2017
Reported
8 Mar 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Cherries

Timeline

17 Feb 2017Recall initiated by company
2 Mar 2017Classified by FDA+13 days
8 Mar 2017Published in enforcement report+6 days

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

Reason for recall

Sunrise Growers is recalling organic IQF Dark Sweet Cherries due to possible Listeria monocytogenes contamination.

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

Organic IQF Dark Sweet Cherries, 900 cartons per lot

Where it was distributed

CA

California

Questions about this recall

Why was it recalled?

Sunrise Growers is recalling organic IQF Dark Sweet Cherries due to possible Listeria monocytogenes contamination.

Which lots are affected?

SWCB62071 PTR160495-28 SWCB62072 PTR160495-28

Where was it sold?

CA

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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