CLASS II Food recall · Reported 10 Jul 2019 · FDA Enforcement Report

Woodstock Organic Grilled Red Pepper recalled by UNFI General Corporate

Unfi General Corporate is recalling Woodstock Organic Grilled Red Pepper, distributed in 29 states. The recall was initiated on 19 Jun 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 60B, Expires April 2020
Quantity recalled1010 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-1527-2019
FDA event ID
83174
Recalling firm
Unfi General Corporate, Providence, RI
Classification
Class II
Status
Terminated
Recall initiated
19 Jun 2019
FDA classified
2 Jul 2019
Reported
10 Jul 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Fish

Timeline

19 Jun 2019Recall initiated by company
2 Jul 2019Classified by FDA+13 days
10 Jul 2019Published in enforcement report+8 days

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

Reason for recall

Product tested positive for 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

WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714. Frozen.

Where it was distributed

AK AL CA CO CT FL GA IA ID IL IN KS MA ME MI MO MT NC NE NH NJ NM NY OH PA RI SC SD TX UT VA WA WY

AlaskaAlabamaCaliforniaColoradoConnecticutFloridaGeorgiaIowaIllinoisKansasMassachusettsMichiganMissouriMontanaNorth CarolinaNebraskaNew HampshireNew JerseyNew MexicoNew York

Questions about this recall

Why was it recalled?

Product tested positive for Listeria monocytogenes.

Which lots are affected?

Lot # 60B, Expires April 2020

Where was it sold?

AK AL CA CO CT FL GA IA ID IL IN KS MA ME MI MO MT NC NE NH NJ NM NY OH PA RI SC SD TX UT VA WA WY

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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