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Use caution Food recall · FDA · Published October 28, 2016

Altamira Boulder Ice Cream Strawberry Recall: Hepatitis A Virus Risk

Altamira Specialty Food Service recalls Boulder Ice Cream Strawberry tubs (2.5 gallons, white top) due to potential Hepatitis A virus contamination from strawberries. Keep frozen at -20°F until 10/20/2016.

🇺🇸 FDA recall #F-1671-2017FoodAltamira Specialty Food Service ›
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Recalling firmAltamira Specialty Food Service6300 E 39th Ave · Denver, CO 80207-1333
✎ GovInfoNow plain-language explainer

What happened, in plain English

Altamira Specialty Food Service is recalling Boulder Ice Cream Strawberry tubs that may contain Hepatitis A virus from contaminated strawberries. This could cause serious illness if consumed. Read more at govinfonow.com/recall/22965-altamira-boulder-ice-cream-strawberry-recall-hepatitis-a-virus-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/22965-altamira-boulder-ice-cream-strawberry-recall-hepatitis-a-virus-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1671-2017

Cite this page

“Altamira Boulder Ice Cream Strawberry Recall: Hepatitis A Virus Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22965-altamira-boulder-ice-cream-strawberry-recall-hepatitis-a-virus-risk. Based on FDA recall #F-1671-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1671-2017%22&limit=1).

Why it’s dangerous

The strawberries used in the ice cream may have been contaminated with Hepatitis A virus, which can cause serious illness including jaundice, fatigue, and abdominal pain. Eating the product could lead to infection if the virus is present.

Who’s affected

People who purchased the Boulder Ice Cream Strawberry tubs (2.5 gallons, white top) between October 2016 and the used-by date. Those who have eaten the product are at risk of Hepatitis A infection.

How to tell if you have this one

Check for Boulder Ice Cream Strawberry tubs with a white top that are 2.5 gallons in size. The product was sold with a used-by date of October 20, 2016.

  • Brand
    Altamira Specialty Food Service
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Date

    Look for the used-by date on the tub, which is October 20, 2016.

  2. Discard if Eaten

    If you consumed the product, contact Altamira Specialty Food Service for guidance.

Where it went and when

Where it was distributed

Distributed in New Mexico.

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: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: yesNMKansas: 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: “New Mexico” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New Mexico.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Oct 28, 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-1671-2017 (October 28, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1671-2017 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