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Lower risk Food recall · FDA · Published September 1, 2019

Apetina Marinated Olives & Feta Recall: Room Temperature Storage Risk

Apetina Marinated Olives & Feta in Olive Oil was recalled due to being held at room temperature instead of refrigerated, posing a food safety risk. Consumers should check UPC 0009393605697 for affected products.

🇺🇸 FDA recall #F-2248-2019FoodApetina ›
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Contact the company

Recalling firmUNFI General Corporate313 Iron Horse Way · Providence, RI 02908-5637
✎ GovInfoNow plain-language explainer

Apetina's marinated olives and feta in olive oil were recalled because they were stored at room temperature instead of refrigerated. This could lead to foodborne illness if the product was consumed after being left out too long. Read more at govinfonow.com/recall/16688-apetina-marinated-olives-feta-recall-room-temperature-storage-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/16688-apetina-marinated-olives-feta-recall-room-temperature-storage-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-2248-2019

Cite this page

“Apetina Marinated Olives & Feta Recall: Room Temperature Storage Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16688-apetina-marinated-olives-feta-recall-room-temperature-storage-risk. Based on FDA recall #F-2248-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2248-2019%22&limit=1).

UNFI General Corporate voluntarily recalled Apetina Marinated Olives & Feta in Olive Oil due to improper storage temperatures, according to the FDA. The Food and Drug Administration announced the recall on September 1, 2019.

How to tell if you have it

  • Brand: Apetina
  • Product: Apetina Marinated Olives & Feta in Olive Oil
  • Packaging: 3.1 LB pals; 4 pals/case
  • UPC: 0009393605697
  • Distribution: KY, IN, IL, MI, FL, OH, MO

The hazard

The product was held at room temperature despite the label stating it should be kept refrigerated. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show UNFI General Corporate has had six other recalls on record since June 19, 2019. Other recent recalls of similar products include Amy's Organic Lentil Light in Sodium Soup Recall (June 22, 2026), Gias Food Lemon Alfredo Fettuccine Recall (Sept. 3, 2026), and Kofinas Garlic Olive Oil Recall (Aug. 29, 2026).

How to tell if you have this one

Check for the UPC code 0009393605697 on the product packaging. The product was sold in 3.1 LB pouches, 4 per case, by UNFI in Greenwood and Sarasota.

  • Brand
    Apetina
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Temperature

    Ensure the product has been refrigerated before consumption.

Where it went and when

Where it was distributed

Distributed in 7 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: 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: yesFL

FDA distribution: “Products distributed in: KY, IN, IL, MI, FL, OH, MO” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Illinois, Indiana, Kentucky, Michigan, Missouri, Ohio.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Sep 1, 201912. FDA classified it Class II: Sep 26, 201923. Published in FDA’s Enforcement Report: Oct 2, 201934. FDA terminated the recall: Nov 10, 2020420192020
  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.

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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-2248-2019 (September 1, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2248-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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