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Stop using now Food recall · FDA · Published July 19, 2016

Gourmet Foods Recalls Artichoke Bottom Ratatouille Due to E. coli Risk

Gourmet Foods, Inc. recalls Artichoke Bottom Ratatouille (UPC 18010-03) due to potential E. coli contamination from flour supplied by General Mills.

🇺🇸 FDA recall #F-0170-2017FoodGourmet Foods ›
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Recalling firmGourmet Foods, Inc.2557 Barrington Ct · Hayward, CA 94545-1174
✎ GovInfoNow plain-language explainer

What happened, in plain English

Gourmet Foods, Inc. has recalled its Artichoke Bottom Ratatouille because the product was manufactured using flour that carries a potential E. coli contamination risk. The affected items were distributed in the California Bay Area and to a single warehouse in Hawaii. The company has not yet provided a specific remedy or return instructions for consumers. Read more at govinfonow.com/recall/23785-gourmet-foods-recalls-artichoke-bottom-ratatouille-due-to-e-coli.

Source Summary by GovInfoNow · govinfonow.com/recall/23785-gourmet-foods-recalls-artichoke-bottom-ratatouille-due-to-e-coli · Updated October 9, 2026 · FDA enforcement record: FDA #F-0170-2017

Cite this page

“Gourmet Foods Recalls Artichoke Bottom Ratatouille Due to E. coli Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23785-gourmet-foods-recalls-artichoke-bottom-ratatouille-due-to-e-coli. Based on FDA recall #F-0170-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0170-2017%22&limit=1).

Why it’s dangerous

The hazard stems from flour used in the manufacturing process that was previously recalled by General Mills due to potential E. coli contamination. Consuming contaminated flour can lead to serious health issues associated with E. coli infection.

Who’s affected

Consumers who purchased the recalled Artichoke Bottom Ratatouille from the California Bay Area or the specific warehouse in Hawaii are at risk of foodborne illness. The product was sold in cases containing 240 pieces each.

How to tell if you have this one

Check for Artichoke Bottom Ratatouille packaged in cases of 240 pieces per case with UPC 18010-03. The product must be kept frozen and bears lot code 129. It was distributed by Gourmet Foods, Inc. in Hayward, CA.

  • Brand
    Gourmet Foods
  • Category
    Food
FDA recall event · 8 products

All 8 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    CA - Bay area and to one firm warehouse in HI but product was not further distributed.
Recall numberProduct, codes & lotsQuantity
F-0169-2017Artichoke Heart Breaded with Goat and Cheddar Cheese : Pack Size: 240 ea. per case; UPC: 13014-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 124, 125.25 cases (240 pieces per case)
F-0170-2017Artichoke Bottom Ratatouille Pack Size: 240 ea. per case UPC: 18010-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 1298 cases (240 pieces per case)
F-0171-2017Artichoke Heart with Boursin Mousse Breaded Pack Size: 200 ea. per case UPC: 11784-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 190, 191, 21539 cases (200 pieces per case)
F-0172-2017Strudel Wild Mushroom Pack Size: 240 ea. per case UPC: 17338-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 119, 214,16 cases (240 pieces per case)
F-0173-2017Breaded Cheese Ravioli Pack Size: 1 oz. ea. 15 lb. per case UPC: 18890-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 364 .6 cases
F-0174-2017Stretched Coconut Shrimp Pack Size: 180 ea. per case UPC: 22102-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 362, 380, 399 .58 cases (180 per case)
F-0175-2017Shrimp Coconut Brochette Pack Size: 156 ea. per case UPC: 23811-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 374, 40315 cases (156 pieces per case)
F-0176-2017Shrimp 21/25 Coconut Butterfly Pack Size: 200 ea. per case UPC: 23502-03 Keep Frozen: Gourmet Foods, Hayward, CA; Lot codes 383, 39732 cases (200 pieces per case)
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Artichoke Bottom Ratatouille due to the potential E. coli contamination risk.

  2. Discard or return items

    The recall record does not specify a remedy, so please check with Gourmet Foods, Inc. for further instructions on disposal or returns.

Where it went and when

Where it was distributed

Distributed in California and Hawaii.

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: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest 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: yesHITexas: not listedTXFlorida: not listedFL

FDA distribution: “CA - Bay area and to one firm warehouse in HI but product was not further distributed.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Hawaii.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jul 19, 201612. FDA classified it Class II: Oct 18, 201623. FDA terminated the recall: Oct 18, 201634. Published in FDA’s Enforcement Report: Oct 26, 201642016
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-0170-2017 (July 19, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0170-2017 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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