CLASS I Food recall · Reported 6 Nov 2013 · FDA Enforcement Report

Red and Green Bell Peppers recalled by Orange County Produce

Orange County Produce is recalling Red and Green Bell Peppers, distributed in California. The recall was initiated on 6 Oct 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # SB 7 920, SB 7 923, SB 7 924
Quantity recalled1208 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-0084-2014
FDA event ID
66453
Recalling firm
Orange County Produce, Irvine, CA
Classification
Class I
Status
Terminated
Recall initiated
6 Oct 2013
FDA classified
28 Oct 2013
Reported
6 Nov 2013
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella
Product category
Peppers

Timeline

6 Oct 2013Recall initiated by company
28 Oct 2013Classified by FDA+22 days
6 Nov 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

Orange County Produce, LLC is recalling fresh red and green Bell Peppers because they may have the potential to be contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Red and Green Bell Peppers, 25 lbs.

Where it was distributed

CA

California

Questions about this recall

Why was it recalled?

Orange County Produce, LLC is recalling fresh red and green Bell Peppers because they may have the potential to be contaminated with Salmonella.

Which lots are affected?

Lot # SB 7 920, SB 7 923, SB 7 924

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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