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Lower risk Food recall · FDA · Published October 8, 2016

Ciao Bovina Italian Strawberry Gelato Recall: Hepatitis A Virus Risk

Ciao Bovina recalls 1 pint Italian strawberry gelato due to potential Hepatitis A virus contamination. Consumers should avoid consumption until notified.

🇺🇸 FDA recall #F-1677-2017FoodCiao Bovina ›
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Contact the company

Recalling firmCiao Bovina, LLC1515 Main Street, #5 · Longmont, CO 80501
✎ GovInfoNow plain-language explainer

What happened, in plain English

Ciao Bovina is recalling 1 pint Italian strawberry gelato that may contain Hepatitis A virus. This could cause liver infection if consumed. The product was sold until November 9, 2016. Read more at govinfonow.com/recall/23055-ciao-bovina-italian-strawberry-gelato-recall-hepatitis-a-virus-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/23055-ciao-bovina-italian-strawberry-gelato-recall-hepatitis-a-virus-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1677-2017

Cite this page

“Ciao Bovina Italian Strawberry Gelato Recall: Hepatitis A Virus Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23055-ciao-bovina-italian-strawberry-gelato-recall-hepatitis-a-virus-risk. Based on FDA recall #F-1677-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1677-2017%22&limit=1).

Why it’s dangerous

Hepatitis A virus can cause liver infection and is spread through contaminated food or water. This gelato may have been contaminated during production, posing a risk if eaten.

Who’s affected

Consumers who purchased the 1 pint (473 ml) Italian strawberry gelato from Ciao Bovina between the product's sale date and November 9, 2016. People with weakened immune systems are at higher risk for infection.

How to tell if you have this one

Look for the product name 'Ciao Bovina Italian Strawberry' on the label. The product is a 1 pint (473 ml) non-dairy gelato with no GMOs, coconut, or soy. It was sold until November 9, 2016.

  • Brand
    Ciao Bovina
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name 'Ciao Bovina Italian Strawberry' and the expiration date of November 9, 2016.

Where it went and when

Where it was distributed

Distributed in Colorado, and outside the U.S.

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: not listedCAUtah: not listedUTColorado: yesCONebraska: 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: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Colorado. No Canadian, other foreign, VA/govt/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Oct 8, 201612. FDA classified it Class I: Mar 21, 201723. Published in FDA’s Enforcement Report: Mar 29, 201734. FDA terminated the recall: May 31, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class I
  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-1677-2017 (October 8, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1677-2017 to see it in context.
  • Plain-language summary written by qwen3:4b 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