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Stop using now Food recall · FDA · Published March 22, 2021

La Fe Frozen Peppers and Onions Recall: Plastic Hazard

Grace Kennedy Foods recalls La Fe Brand Frozen Peppers and Onions due to plastic contamination. Check lot KR043021.

🇺🇸 FDA recall #F-0362-2021FoodLa Fe ›
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Recalling firmGrace Kennedy Foods USA LLC5 Ethel Blvd · Wood Ridge, NJ 07075-2431
✎ GovInfoNow plain-language explainer

What happened, in plain English

Grace Kennedy Foods USA LLC is recalling 16 oz bags of La Fe Brand Frozen Peppers and Onions because they may contain pieces of plastic. The affected product was distributed to retail stores in Connecticut, Delaware, Massachusetts, New Jersey, New York, and Pennsylvania. The specific lot number involved is KR043021. Read more at govinfonow.com/recall/14750-la-fe-frozen-peppers-and-onions-recall-plastic-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/14750-la-fe-frozen-peppers-and-onions-recall-plastic-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-0362-2021

Cite this page

“La Fe Frozen Peppers and Onions Recall: Plastic Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/14750-la-fe-frozen-peppers-and-onions-recall-plastic-hazard. Based on FDA recall #F-0362-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0362-2021%22&limit=1).

Why it’s dangerous

The presence of plastic in the food product poses a choking hazard or potential injury if swallowed. Ingesting foreign objects like plastic can cause serious internal damage or require medical intervention.

Who’s affected

Consumers who purchased 16 oz bags of La Fe Brand Frozen Peppers and Onions from retail stores in CT, DE, MA, NJ, NY, or PA. Anyone who bought the specific lot KR043021 is at risk of ingesting plastic.

How to tell if you have this one

Look for 16 oz bags of La Fe Brand Frozen Peppers and Onions with Lot # KR043021 and Batch # K10605. These items were sold in retail stores across Connecticut, Delaware, Massachusetts, New Jersey, New York, and Pennsylvania.

  • Brand
    La Fe
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the frozen peppers and onions if you have the recalled lot.

  2. Discard or return the item

    The record does not specify a remedy, so please discard the product or contact the retailer for assistance.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: yesDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed to retail stores in CT, DE, MA, NJ, NY, and PA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, Delaware, Massachusetts, New Jersey, New York, Pennsylvania.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Mar 22, 202112. FDA classified it Class II: Mar 26, 202123. Published in FDA’s Enforcement Report: Apr 7, 202134. FDA terminated the recall: Mar 25, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

How many cases were recalled?

A total of 187 cases, containing 12 bags per case, were part of this recall.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0362-2021 (March 22, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0362-2021 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA