CLASS II Food recall · Reported 5 Feb 2014 · FDA Enforcement Report

California Girl canned Peach Halves in Juice recalled

Atlapac Trading is recalling California Girl canned Peach Halves in Juice, distributed in California. The recall was initiated on 14 Nov 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesCode: 3700/01182 OCT.-08-2012 OCT.-08-2015
Quantity recalled881 units

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-1439-2014
FDA event ID
66858
Recalling firm
Atlapac Trading, Commerce, CA
Classification
Class II
Status
Terminated
Recall initiated
14 Nov 2013
FDA classified
24 Jan 2014
Reported
5 Feb 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Juice

Timeline

14 Nov 2013Recall initiated by company
24 Jan 2014Classified by FDA+71 days
5 Feb 2014Published 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

Atlapac Trading Co. is recalling California Girl canned Peach Halves because they were reported to be swollen.

Product as listed by the FDA

California Girl canned Peach Halves in Juice, 6 cans per case. UPC 52391 72992

Where it was distributed

CA

California

Questions about this recall

Why was it recalled?

Atlapac Trading Co. is recalling California Girl canned Peach Halves because they were reported to be swollen.

Which lots are affected?

Code: 3700/01182 OCT.-08-2012 OCT.-08-2015

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 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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