CLASS II Food recall · Reported 11 Dec 2013 · FDA Enforcement Report

Korean Pear Juice single service container recalled

Evergreen Orchard Farm is recalling Korean Pear Juice single service container, distributed in Maryland, New Jersey, New York, Virginia. The recall was initiated on 16 Mar 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesN/A
Quantity recalledUnknown

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-1341-2012
FDA event ID
61777
Recalling firm
Evergreen Orchard Farm, Hamilton, NJ
Classification
Class II
Status
Terminated
Recall initiated
16 Mar 2012
FDA classified
2 Dec 2013
Reported
11 Dec 2013
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors
Product category
Juice

Timeline

16 Mar 2012Recall initiated by company
2 Dec 2013Classified by FDA+626 days
11 Dec 2013Published in enforcement report+9 days

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

Reason for recall

Juice and paste products display incorrect labeling, product descriptions and formulations.

Product as listed by the FDA

Korean Pear Juice in 120 mL metal foil pouch single service container. Made by Evergreen Orchard Farm, 1023 Yardville Allentown Road, Hamilton, NJ 08620. Product of USA. UPC# 809080300084.

Where it was distributed

New Jersey, New York, Virginia and Maryland.

MarylandNew JerseyNew YorkVirginia

Questions about this recall

Why was it recalled?

Juice and paste products display incorrect labeling, product descriptions and formulations.

Which lots are affected?

N/A

Where was it sold?

New Jersey, New York, Virginia and Maryland.

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.

Other products in this recall event

3 other products · FDA event 61777

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