CLASS II Food recall · Reported 7 Apr 2021 · FDA Enforcement Report

La Fe Frozen Peppers and Onions recalled by Grace Kennedy Foods USA

Grace Kennedy Foods USA is recalling La Fe Frozen Peppers and Onions, distributed in Connecticut, Delaware, Massachusetts, New Jersey, New York, Pennsylvania. The recall was initiated on 22 Mar 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLOT # KR043021, Batch # K10605
Quantity recalled187 CASES (12 bags per case)

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-0362-2021
FDA event ID
87573
Recalling firm
Grace Kennedy Foods USA, Wood Ridge, NJ
Brand
La Fe
Classification
Class II
Status
Terminated
Recall initiated
22 Mar 2021
FDA classified
26 Mar 2021
Reported
7 Apr 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Product category
Onions

Timeline

22 Mar 2021Recall initiated by company
26 Mar 2021Classified by FDA+4 days
7 Apr 2021Published 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

Presence of plastic in bagged frozen peppers and onions.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

La Fe Brand Frozen Peppers and Onions 16 oz bags.

Where it was distributed

Distributed to retail stores in CT, DE, MA, NJ, NY, and PA

ConnecticutDelawareMassachusettsNew JerseyNew YorkPennsylvania

Questions about this recall

Why was it recalled?

Presence of plastic in bagged frozen peppers and onions.

Which lots are affected?

LOT # KR043021, Batch # K10605

Where was it sold?

Distributed to retail stores in CT, DE, MA, NJ, NY, and PA

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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